-
1
-
-
0028116218
-
Idiopathic dilated cardiomyopathy
-
Dec, G.W. and Fuster, V. 1994. Idiopathic dilated cardiomyopathy. N. Engl. J. Med. 331:1564-1575.
-
(1994)
N. Engl. J. Med.
, vol.331
, pp. 1564-1575
-
-
Dec, G.W.1
Fuster, V.2
-
2
-
-
0026629099
-
Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute Workshop)
-
Manolio, T.A., Baughman, K.L., Rodeheffer, R., Pearson, T.A., and Bristow, J.D. 1992. Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute Workshop). Am. J. Cardiol. 69:1458-1466.
-
(1992)
Am. J. Cardiol.
, vol.69
, pp. 1458-1466
-
-
Manolio, T.A.1
Baughman, K.L.2
Rodeheffer, R.3
Pearson, T.A.4
Bristow, J.D.5
-
3
-
-
0024422923
-
Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study of Olmsted County, Minnesota, 1975-1984
-
Codd, M.B., Sugrue, D.D., Gersh, B.J., and Melton, L.J. 1989. Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study of Olmsted County, Minnesota, 1975-1984. Circulation. 80:564-572.
-
(1989)
Circulation
, vol.80
, pp. 564-572
-
-
Codd, M.B.1
Sugrue, D.D.2
Gersh, B.J.3
Melton, L.J.4
-
4
-
-
0028041629
-
Economic impact of heart failure in the United States: Time for a different approach
-
O'Connell, J.B., and Bristow, M.R. 1994. Economic impact of heart failure in the United States: time for a different approach. J. Heart Lung Transplant. 13:S10-S112.
-
(1994)
J. Heart Lung Transplant
, vol.13
-
-
O'Connell, J.B.1
Bristow, M.R.2
-
5
-
-
0028295899
-
The causes dilated cardiomyopathy: A clinicopathologic review of 673 consecutive patients
-
Kasper, E.K., et al. 1994. The causes dilated cardiomyopathy: a clinicopathologic review of 673 consecutive patients. J. Am. Coll. Cardiol. 23:586-590.
-
(1994)
J. Am. Coll. Cardiol.
, vol.23
, pp. 586-590
-
-
Kasper, E.K.1
-
6
-
-
0032947130
-
Pediatric myocardial disease
-
Towbin, J.A. 1999. Pediatric myocardial disease. Pediatr. Clin. North. Am. 46:289-312.
-
(1999)
Pediatr. Clin. North. Am.
, vol.46
, pp. 289-312
-
-
Towbin, J.A.1
-
7
-
-
0026319459
-
The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
-
Michels, V.V., et al. 1992. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. N. Engl. J. Med. 326:77-82.
-
(1992)
N. Engl. J. Med.
, vol.326
, pp. 77-82
-
-
Michels, V.V.1
-
8
-
-
0029009393
-
Familial dilated cardiomyopathy in the United Kingdom
-
Keeling, P.J., et al. 1995. Familial dilated cardiomyopathy in the United Kingdom. Br. Heart J. 73:417-421.
-
(1995)
Br. Heart J.
, vol.73
, pp. 417-421
-
-
Keeling, P.J.1
-
9
-
-
0031951537
-
Frequency and phenotypes of familial dilated cardiomyopathy
-
Grunig, E., et al. 1998. Frequency and phenotypes of familial dilated cardiomyopathy. J. Am. Coll. Cardiol. 31:186-194.
-
(1998)
J. Am. Coll. Cardiol.
, vol.31
, pp. 186-194
-
-
Grunig, E.1
-
10
-
-
0027215234
-
Molecular genetic aspects of cardiomyopathy
-
Towbin, J.A. 1993. Molecular genetic aspects of cardiomyopathy. Biochem. Med. Metab. Biol. 49:285-300.
-
(1993)
Biochem. Med. Metab. Biol.
, vol.49
, pp. 285-300
-
-
Towbin, J.A.1
-
11
-
-
0029963145
-
A novel X-linked gene, G4.5. is responsible for Barth syndrome
-
Bione, S., et al. 1996. A novel X-linked gene, G4.5. is responsible for Barth syndrome. Nat. Genet. 12:385-389.
-
(1996)
Nat. Genet.
, vol.12
, pp. 385-389
-
-
Bione, S.1
-
12
-
-
0030728921
-
Mutation characterization and genotype-phenotype correlation in Barth syndrome
-
Johnston, J., et al. 1997. Mutation characterization and genotype-phenotype correlation in Barth syndrome, Am. Hum. Genet. 61:1053-1058.
-
(1997)
Am. Hum. Genet.
, vol.61
, pp. 1053-1058
-
-
Johnston, J.1
-
13
-
-
16944366521
-
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies
-
D'Adamo, P., et al. 1997. The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. Am. J. Hum. Genet. 61:862-867.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 862-867
-
-
D'Adamo, P.1
-
14
-
-
0030774767
-
Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome
-
Bleyl, S.B., et al. 1997. Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome. Am. J. Hum. Genet. 61:868-872.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 868-872
-
-
Bleyl, S.B.1
-
15
-
-
0027193330
-
X-linked dilated cardiomyopathy: Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
-
Towbin, J.A., et al. 1993. X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation. 87:1854-1865.
-
(1993)
Circulation
, vol.87
, pp. 1854-1865
-
-
Towbin, J.A.1
-
16
-
-
0027265702
-
Brief report: Deletion of the dystrophin muscle-specific promoter region associated with X-linked dilated cardiomyopathy
-
Muntoni, F., et al. 1993. Brief report: deletion of the dystrophin muscle-specific promoter region associated with X-linked dilated cardiomyopathy. N. Engl. J. Med. 329:921-925.
-
(1993)
N. Engl. J. Med.
, vol.329
, pp. 921-925
-
-
Muntoni, F.1
-
17
-
-
0030922569
-
Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy
-
Ortiz-Lopez, R., Li, H., Su, J., Goytia, V., and Towbin, J.A. 1997. Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy. Circulation. 95:2434-2440.
-
(1997)
Circulation
, vol.95
, pp. 2434-2440
-
-
Ortiz-Lopez, R.1
Li, H.2
Su, J.3
Goytia, V.4
Towbin, J.A.5
-
18
-
-
0028801254
-
Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32
-
Durand, J.B., et al. 1995. Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32. Circulation. 92:3387-3389.
-
(1995)
Circulation
, vol.92
, pp. 3387-3389
-
-
Durand, J.B.1
-
19
-
-
0033514986
-
Familial dilated cardiomyopathy locus maps to chromosome 2q31
-
Siu, B.L., et al. 1999. Familial dilated cardiomyopathy locus maps to chromosome 2q31. Circulation. 99:1022-1026.
-
(1999)
Circulation
, vol.99
, pp. 1022-1026
-
-
Siu, B.L.1
-
20
-
-
0029151478
-
Linkage of familial dilated cardiomyopathy to chromosome 9
-
Krajinovic, M., et al. 1995. Linkage of familial dilated cardiomyopathy to chromosome 9. Am. J. Hum. Genet. 57:846-852.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 846-852
-
-
Krajinovic, M.1
-
21
-
-
0029784361
-
Gene mapping of Famalial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23
-
Bowles, K.R., et al. 1996. Gene mapping of Famalial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23. J. Clin. Invest. 98:1355-1360.
-
(1996)
J. Clin. Invest.
, vol.98
, pp. 1355-1360
-
-
Bowles, K.R.1
-
22
-
-
0032076955
-
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
-
Olson, T.M., Michels, V.A., Thibodeau, S.N., Tai, Y.S., and Keating, M.T. 1998. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science. 280:750-752.
-
(1998)
Science
, vol.280
, pp. 750-752
-
-
Olson, T.M.1
Michels, V.A.2
Thibodeau, S.N.3
Tai, Y.S.4
Keating, M.T.5
-
23
-
-
0028145745
-
A genetic defect that causes conduction system disease and dilated cardiomyopathy maps to 1p1-1q1
-
Kass, S., et al. 1994. A genetic defect that causes conduction system disease and dilated cardiomyopathy maps to 1p1-1q1. Natl. Genet. 7:546-551.
-
(1994)
Natl. Genet.
, vol.7
, pp. 546-551
-
-
Kass, S.1
-
24
-
-
0033358083
-
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22
-
Jung, M., et al. 1999. Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22. Am. J. Hum. Genet. 65:1068-1077.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1068-1077
-
-
Jung, M.1
-
25
-
-
0033520037
-
Desmin mutation responsible for idiopathic dilated cardiomyopathy
-
Li, D., et al. 1999. Desmin mutation responsible for idiopathic dilated cardiomyopathy. Circulation. 100:461-464.
-
(1999)
Circulation
, vol.100
, pp. 461-464
-
-
Li, D.1
-
26
-
-
0030031004
-
Mapping a cardiomyopathy locus to chromosome 3p22-p25
-
Olson, T.M., and Keating, M.T. 1996. Mapping a cardiomyopathy locus to chromosome 3p22-p25. J. Clin. Invest. 97:528-532.
-
(1996)
J. Clin. Invest.
, vol.97
, pp. 528-532
-
-
Olson, T.M.1
Keating, M.T.2
-
27
-
-
0030882270
-
Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23
-
Messina, D.N., Speer, M.C., Pericak-Vance, M.A., and McNally, E.M. 1997. Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. Am. J. Hum. Genet. 61:909-917.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 909-917
-
-
Messina, D.N.1
Speer, M.C.2
Pericak-Vance, M.A.3
McNally, E.M.4
-
28
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction system disease
-
Fatkin, D., et al. 1999. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction system disease. N. Engl. J. Med. 341:1715-1724.
-
(1999)
N. Engl. J. Med.
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
-
29
-
-
0033051753
-
Etiologies of cardiomyopathy and heart failure
-
Towbin, J.A., Bewies, K.R., and Bowles, N.E. 1999. Etiologies of cardiomyopathy and heart failure. Nat. Med. 3:266-267.
-
(1999)
Nat. Med.
, vol.3
, pp. 266-267
-
-
Towbin, J.A.1
Bewies, K.R.2
Bowles, N.E.3
-
30
-
-
0032006681
-
The role of cytoskoletal proteins in cardiomyopathy
-
Towbin, J.A. 1998. The role of cytoskoletal proteins in cardiomyopathy. Curr. Opin. Cell. Biol. 10:131-139.
-
(1998)
Curr. Opin. Cell. Biol.
, vol.10
, pp. 131-139
-
-
Towbin, J.A.1
-
31
-
-
0032555955
-
Familial hypertrophic cardiomyopathy: From mutations to functional defects
-
Bonne, G., Carrier, L., Richard, P., Hainque, B., and Schwartz, K. 1998. Familial hypertrophic cardiomyopathy: from mutations to functional defects. Circ. Res. 83:580-593.
-
(1998)
Circ. Res.
, vol.83
, pp. 580-593
-
-
Bonne, G.1
Carrier, L.2
Richard, P.3
Hainque, B.4
Schwartz, K.5
-
32
-
-
0031707743
-
The molecular basis of long QT syndrome and prospects for therapy
-
Wang, Q., Bowles, N.E., and Towbin, JA 1998. The molecular basis of long QT syndrome and prospects for therapy. Mol. Med. Today. 4:382-388.
-
(1998)
Mol. Med. Today
, vol.4
, pp. 382-388
-
-
Wang, Q.1
Bowles, N.E.2
Towbin, J.A.3
-
33
-
-
0014696557
-
Spontaneous, hereditary myocardial degeneration and congestive heart failure in a strain of Syrian hamsters
-
Bajusz, E., Baker, J.R., Nixon, C.W., and Homburger, F. 1969. Spontaneous, hereditary myocardial degeneration and congestive heart failure in a strain of Syrian hamsters. Ann NY Acad. Sci. 156:105-129.
-
(1969)
Ann NY Acad. Sci.
, vol.156
, pp. 105-129
-
-
Bajusz, E.1
Baker, J.R.2
Nixon, C.W.3
Homburger, F.4
-
34
-
-
84985494028
-
Myopathy of hamster dystrophy: History and morphologic aspects
-
Homburger, F. 1979. Myopathy of hamster dystrophy: history and morphologic aspects. Ann. NY Acad. Sci. 317:1-17.
-
(1979)
Ann. NY Acad. Sci.
, vol.317
, pp. 1-17
-
-
Homburger, F.1
-
35
-
-
0031471956
-
Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex
-
Sakamoto A., et al. 1997. Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, δ-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex. Proc. Natl. Acad. Sci. USA. 94:13873-13878.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 13873-13878
-
-
Sakamoto, A.1
-
36
-
-
8244259185
-
Identification of the Syrian hamster cardiomyopathy gene
-
Nigro, V., et al. 1997. Identification of the Syrian hamster cardiomyopathy gene. Hum. Mol. Genet. 6:601-607.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 601-607
-
-
Nigro, V.1
-
37
-
-
0032973716
-
Delineation of genomic deletion in cardiomyopathic hamster
-
Sakamoto, A., Abe, M., and Masaki, T. 1999. Delineation of genomic deletion in cardiomyopathic hamster. FEBS Lett. 447:124-128.
-
(1999)
FEBS Lett.
, vol.447
, pp. 124-128
-
-
Sakamoto, A.1
Abe, M.2
Masaki, T.3
-
38
-
-
0031795402
-
Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster
-
Straub, V. 1998. Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster. Am. J. Pathol. 153:1623-1630.
-
(1998)
Am. J. Pathol.
, vol.153
, pp. 1623-1630
-
-
Straub, V.1
-
39
-
-
0029816797
-
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
-
Nigro, V., et al. 1996. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene. Nat. Genet. 14:195-198.
-
(1996)
Nat. Genet.
, vol.14
, pp. 195-198
-
-
Nigro, V.1
-
40
-
-
0031764046
-
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limbgirdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies
-
Moreira, E.S., et al. 1998. A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limbgirdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies. J. Med. Genet. 35:951-953.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 951-953
-
-
Moreira, E.S.1
-
41
-
-
0032912836
-
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations
-
Melacini, P., et al. 1999. Heart involvement in muscular dystrophies due to sarcoglycan gene mutations. Muscle Nerve. 22:473-479.
-
(1999)
Muscle Nerve
, vol.22
, pp. 473-479
-
-
Melacini, P.1
-
42
-
-
0024595101
-
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
-
Orita, M., Iwahana, H., Kanazawa, H., Hayashi, K., and Sekiya, T. 1989. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc. Natl. Acad. Sci. USA. 86:2766-2770.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 2766-2770
-
-
Orita, M.1
Iwahana, H.2
Kanazawa, H.3
Hayashi, K.4
Sekiya, T.5
-
43
-
-
0017873321
-
Analyses of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins
-
Garmier J., Osguthorpe, D.J., and Robson, B. 1978. Analyses of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins. J. Biol. Chem. 120:97-120.
-
(1978)
J. Biol. Chem.
, vol.120
, pp. 97-120
-
-
Garmier, J.1
Osguthorpe, D.J.2
Robson, B.3
-
44
-
-
10144247267
-
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein
-
Nigro, V., et al. 1996. Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein. Hum. Mol. Genet. 5:1179-1186.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1179-1186
-
-
Nigro, V.1
-
45
-
-
10544235436
-
Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy
-
Jung, D., et al. 1996. Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy. J. Biol. Chem. 271:32321-32329.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 32321-32329
-
-
Jung, D.1
-
46
-
-
0026086794
-
Idiopathic dilated cardiomyopathy. An immunologic, genetic, or infectious disease, or all of the above?
-
Bender, J.R. 1991. Idiopathic dilated cardiomyopathy. An immunologic, genetic, or infectious disease, or all of the above? Circulation. 83:515-522.
-
(1991)
Circulation
, vol.83
, pp. 515-522
-
-
Bender, J.R.1
-
47
-
-
18744433901
-
α-cardiac actin is a novel gene in familial hypertrophic cardiomyopathy
-
Mogensen, J., et al. 1999. α-cardiac actin is a novel gene in familial hypertrophic cardiomyopathy. J. Clin. Invest. 103:R39-R43.
-
(1999)
J. Clin. Invest.
, vol.103
-
-
Mogensen, J.1
-
48
-
-
0033361893
-
Towards an understanding of the cause of mitral valve prolapse
-
Towbin, J.A. 1999. Towards an understanding of the cause of mitral valve prolapse. Am. J. Hum. Genet. 65:1238-1241.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1238-1241
-
-
Towbin, J.A.1
-
49
-
-
0023614188
-
Dystrophin: The protein product of the Duchenne muscular dystrophy locus
-
Hoffman, E.P., Brown, R.H., and Kunkel, L.M. 1987. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell. 51:919-928.
-
(1987)
Cell
, vol.51
, pp. 919-928
-
-
Hoffman, E.P.1
Brown, R.H.2
Kunkel, L.M.3
-
50
-
-
0031722943
-
The sarcoglycan complex in limb-girdle muscular dystrophy
-
Lim, L.E., and Campbell, K.P. 1998. The sarcoglycan complex in limb-girdle muscular dystrophy. Curr. Opin. Neurol. 11:443-452.
-
(1998)
Curr. Opin. Neurol.
, vol.11
, pp. 443-452
-
-
Lim, L.E.1
Campbell, K.P.2
-
51
-
-
0033183434
-
Sarcoglycan complex: A muscular supporter of dystroglycan-dystrophin interplay?
-
Matsumura, K., et al. 1999. Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay? Cell. Mol. Biol. 45:751-762.
-
(1999)
Cell. Mol. Biol.
, vol.45
, pp. 751-762
-
-
Matsumura, K.1
-
52
-
-
0002111569
-
Biochemical and molecular characterization of X-linked dilated cardiomyopathy (XLCM)
-
E.B. Clark, R.R. Markwald, and A. Takao, editors, Futura Publishing Co. New York, New York, USA
-
Towbin, J.A. 1995. Biochemical and molecular characterization of X-linked dilated cardiomyopathy (XLCM). In Developmental mechanisms of heart disease. E.B. Clark, R.R. Markwald, and A. Takao, editors, Futura Publishing Co. New York, New York, USA. 121-132.
-
(1995)
Developmental Mechanisms of Heart Disease
, pp. 121-132
-
-
Towbin, J.A.1
-
53
-
-
0032858915
-
Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy
-
Nowak, K.J., et al. 1999. Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy. Nat. Genet. 23:208-212.
-
(1999)
Nat. Genet.
, vol.23
, pp. 208-212
-
-
Nowak, K.J.1
-
54
-
-
0032977685
-
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
-
Bonne, G., et al. 1999. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat. Genet. 21:285-288.
-
(1999)
Nat. Genet.
, vol.21
, pp. 285-288
-
-
Bonne, G.1
-
55
-
-
0033927867
-
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy
-
Raffaele Di Barletta, M., et al. 2000. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. Am. J. Hum. Genet. 66:1407-1412.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1407-1412
-
-
Raffaele Di Barletta, M.1
-
56
-
-
0029816797
-
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene
-
Nigro, V., et al. 1996. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene. Nat. Genet. 14:195-198.
-
(1996)
Nat. Genet.
, vol.14
, pp. 195-198
-
-
Nigro, V.1
-
57
-
-
0031128814
-
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)
-
Duggan, D.J., et al. 1997. Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2). Neurogenetics. 1:49-58.
-
(1997)
Neurogenetics
, vol.1
, pp. 49-58
-
-
Duggan, D.J.1
-
58
-
-
0034702027
-
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
-
Muchir, A., et al. 2000. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Hum. Mol. Genet. 9:1453-1459.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1453-1459
-
-
Muchir, A.1
-
59
-
-
0031920515
-
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy
-
Minetti, C., et al. 1998. Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Nat. Genet. 18:365-368.
-
(1998)
Nat. Genet.
, vol.18
, pp. 365-368
-
-
Minetti, C.1
-
60
-
-
0032494165
-
Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin
-
Hack, A.A., et al. 1998. Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin. J. Cell. Biol. 142:1279-1287.
-
(1998)
J. Cell. Biol.
, vol.142
, pp. 1279-1287
-
-
Hack, A.A.1
-
61
-
-
0033588050
-
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: A novel mechanism for cardiomyopathy and muscular dystrophy
-
Coral-Vazquez, R., et al. 1999. Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy. Cell. 98:465-474.
-
(1999)
Cell
, vol.98
, pp. 465-474
-
-
Coral-Vazquez, R.1
-
62
-
-
0032735294
-
Cardiomyopathy in Duchenne, Becker, and sarcoglycanopathies: A role for coronary dysfunction?
-
Gnecchi-Ruscone, T., et al. 1999. Cardiomyopathy in Duchenne, Becker, and sarcoglycanopathies: a role for coronary dysfunction? Muscle Nerve. 22:1549-1556.
-
(1999)
Muscle Nerve
, vol.22
, pp. 1549-1556
-
-
Gnecchi-Ruscone, T.1
-
63
-
-
0032829045
-
Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice
-
Araishi, K., et al. 1999. Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice. Hum. Mol. Genet. 8:1589-1598.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1589-1598
-
-
Araishi, K.1
|