-
1
-
-
0032563559
-
Microinjection of anticoilin antibodies affects the structure of coiled bodies
-
Almeida F., Saffrich R., Ansorge W., Carmo-Fonseca M. Microinjection of anticoilin antibodies affects the structure of coiled bodies. J. Cell Biol. 142:1998;899-912.
-
(1998)
J. Cell Biol.
, vol.142
, pp. 899-912
-
-
Almeida, F.1
Saffrich, R.2
Ansorge, W.3
Carmo-Fonseca, M.4
-
2
-
-
0032919203
-
The RNA-binding properties of SMN: Deletion analysis of the zebrafish orthologue defines domains conserved in evolution
-
Bertrandy S., Burlet P., Clermont O., Huber C., Fondrat C., Thierry-Mieg D., Munnich A., Lefebvre S. The RNA-binding properties of SMN: Deletion analysis of the zebrafish orthologue defines domains conserved in evolution. Hum. Mol. Genet. 8:1999;775-782.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 775-782
-
-
Bertrandy, S.1
Burlet, P.2
Clermont, O.3
Huber, C.4
Fondrat, C.5
Thierry-Mieg, D.6
Munnich, A.7
Lefebvre, S.8
-
3
-
-
0028882193
-
Mutational analysis of P80 coilin indicates a functional interaction between coiled bodies and the nucleolus
-
Bohmann K., Ferreira J. A., Lamond A. I. Mutational analysis of P80 coilin indicates a functional interaction between coiled bodies and the nucleolus. J. Cell Biol. 131:1995;817-831.
-
(1995)
J. Cell Biol.
, vol.131
, pp. 817-831
-
-
Bohmann, K.1
Ferreira, J.A.2
Lamond, A.I.3
-
4
-
-
0029803986
-
Frameshift mutation in the survival of motor neuron gene in a severe case of SMA type I
-
Brahe C., Clermont O., Zappata S., Tiziano F., Melki J., Neri G. Frameshift mutation in the survival of motor neuron gene in a severe case of SMA type I. Hum. Mol. Genet. 5:1996;1971-1976.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1971-1976
-
-
Brahe, C.1
Clermont, O.2
Zappata, S.3
Tiziano, F.4
Melki, J.5
Neri, G.6
-
5
-
-
0030863569
-
When is deletion not a deletion? When it is converted
-
Burghes A. H. M. When is deletion not a deletion? When it is converted. Am. J. Hum. Genet. 61:1997;9-15.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 9-15
-
-
Burghes, A.H.M.1
-
6
-
-
0029880997
-
Large scale deletions of the 5q12 region are specific to Werdnig-Hoffmann disease
-
Burlet P., Burglen L., Clermont O., Lefebvre S., Viollet L., Munnich A., Melki J. Large scale deletions of the 5q12 region are specific to Werdnig-Hoffmann disease. J. Med. Genet. 33:1996;281-283.
-
(1996)
J. Med. Genet.
, vol.33
, pp. 281-283
-
-
Burlet, P.1
Burglen, L.2
Clermont, O.3
Lefebvre, S.4
Viollet, L.5
Munnich, A.6
Melki, J.7
-
7
-
-
7844249275
-
The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy
-
Burlet P., Huber C., Bertrandy S., Ludosky M. A., Zwaenepoel I., Clermont O., Roume J., Delezoide A. L., Cartaud J., Munnich A., Lefebvre S. The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy. Hum. Mol. Genet. 7:1998;1927-1933.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1927-1933
-
-
Burlet, P.1
Huber, C.2
Bertrandy, S.3
Ludosky, M.A.4
Zwaenepoel, I.5
Clermont, O.6
Roume, J.7
Delezoide, A.L.8
Cartaud, J.9
Munnich, A.10
Lefebvre, S.11
-
8
-
-
0030818315
-
Genomic variation and gene conversion in spinal muscular atrophy: Implications for disease process and clinical phenotype
-
Campbell L., Potter A, Ignatius J., Dubowitz V., Davies K. Genomic variation and gene conversion in spinal muscular atrophy: Implications for disease process and clinical phenotype. Am. J. Hum. Genet. 61:1997;40-50.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 40-50
-
-
Campbell, L.1
Potter, A.2
Ignatius, J.3
Dubowitz, V.4
Davies, K.5
-
9
-
-
8544283791
-
The survival of motor neuron protein in spinal muscular atrophy
-
Coovert D., Le T. T., McAndrew P. E., Strasswimmer J., Crawford T. O., Mendell J. R., Coulson S., Androphy E. J., Prior T. W., Burghes A. H. M. The survival of motor neuron protein in spinal muscular atrophy. Hum. Mol. Genet. 6:1997;1205-1214.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1205-1214
-
-
Coovert, D.1
Le, T.T.2
McAndrew, P.E.3
Strasswimmer, J.4
Crawford, T.O.5
Mendell, J.R.6
Coulson, S.7
Androphy, E.J.8
Prior, T.W.9
Burghes, A.H.M.10
-
10
-
-
0342676120
-
-
DiDonato C., Ingraham S. E., Mendell J. R., Prior T. W., Lenard S., Moxley R. T., Florence J., Burghes A. H. M. Ann. Neurol. 41:1997.
-
(1997)
Ann. Neurol.
, vol.41
-
-
Didonato, C.1
Ingraham, S.E.2
Mendell, J.R.3
Prior, T.W.4
Lenard, S.5
Moxley, R.T.6
Florence, J.7
Burghes, A.H.M.8
-
11
-
-
0030928716
-
The SMN-SIP1 complex has an essential role in spliceosomal snRNP biosynthesis
-
Fischer U., Liu Q., Dreyfuss D. The SMN-SIP1 complex has an essential role in spliceosomal snRNP biosynthesis. Cell. 90:1997;1023-1029.
-
(1997)
Cell
, vol.90
, pp. 1023-1029
-
-
Fischer, U.1
Liu, Q.2
Dreyfuss, D.3
-
12
-
-
0032568567
-
Heterogeneity of subcellular localization and electrophoretic mobility of survival motor neuron (SMN) protein in mammalian neural cells and tissues
-
Francis J. W., Sandrock A. W., Bhide P. G., Vonsattel J. P., Brown R. H. Heterogeneity of subcellular localization and electrophoretic mobility of survival motor neuron (SMN) protein in mammalian neural cells and tissues. Proc. Natl. Acad. Sci. USA. 95:1998;6492-6497.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 6492-6497
-
-
Francis, J.W.1
Sandrock, A.W.2
Bhide, P.G.3
Vonsattel, J.P.4
Brown, R.H.5
-
13
-
-
0031586612
-
Multiple protein:protein interactions between the snRNP common core proteins
-
Fury M. G., Zhang W., Christodoulopoulos I., Zieve G. W. Multiple protein:protein interactions between the snRNP common core proteins. Exp. Cell Res. 237:1997;63-69.
-
(1997)
Exp. Cell Res.
, vol.237
, pp. 63-69
-
-
Fury, M.G.1
Zhang, W.2
Christodoulopoulos, I.3
Zieve, G.W.4
-
14
-
-
0029147787
-
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients
-
Gennarelli M., Lacarelli M., Capon F., Pizzuti A., Merlini L., Angelini C., Novelli G., Dallapiccola B. Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients. Biochem. Biophys. Res. Commun. 213:1995;342-348.
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.213
, pp. 342-348
-
-
Gennarelli, M.1
Lacarelli, M.2
Capon, F.3
Pizzuti, A.4
Merlini, L.5
Angelini, C.6
Novelli, G.7
Dallapiccola, B.8
-
15
-
-
0030987818
-
Missense mutations in exon 6 of the survival of motor neuron gene in patients with spinal muscular atrophy (SMA)
-
Hahnen E., Schonling J., Rudnik-Schoneborn S., Raschke H., Zerres K., Wirth B. Missense mutations in exon 6 of the survival of motor neuron gene in patients with spinal muscular atrophy (SMA). Hum. Mol. Genet. 6:1997;821-825.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 821-825
-
-
Hahnen, E.1
Schonling, J.2
Rudnik-Schoneborn, S.3
Raschke, H.4
Zerres, K.5
Wirth, B.6
-
16
-
-
0029858451
-
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: New insights into molecular mechanisms responsible for the disease
-
Hahnen E., Schonling J., Rudnik-Schoneborn S., Zerres K., Wirth B. Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the disease. Am. J. Hum. Genet. 59:1996;1057-1065.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 1057-1065
-
-
Hahnen, E.1
Schonling, J.2
Rudnik-Schoneborn, S.3
Zerres, K.4
Wirth, B.5
-
17
-
-
0030981541
-
Correlation between severity and SMN protein level in spinal muscular atrophy
-
Lefebvre S., Burlet P., Liu Q., Bertrandy S., Clermont O., Munnich A., Dreyfuss G., Melki J. Correlation between severity and SMN protein level in spinal muscular atrophy. Nature Genet. 16:1997;265-269.
-
(1997)
Nature Genet.
, vol.16
, pp. 265-269
-
-
Lefebvre, S.1
Burlet, P.2
Liu, Q.3
Bertrandy, S.4
Clermont, O.5
Munnich, A.6
Dreyfuss, G.7
Melki, J.8
-
18
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
Lefebvre S., Burglen L., Reboullet S., Clermont O., Burlet P., Viollet L., Benichou B., Cruaud C., Millasseau P., Zevianni M., Le Paslier D., Frezal J., Cohen D., Weissenbach J., Munnich A., Melki J. Identification and characterization of a spinal muscular atrophy-determining gene. Cell. 80:1995;155-165.
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
Burglen, L.2
Reboullet, S.3
Clermont, O.4
Burlet, P.5
Viollet, L.6
Benichou, B.7
Cruaud, C.8
Millasseau, P.9
Zevianni, M.10
Le Paslier, D.11
Frezal, J.12
Cohen, D.13
Weissenbach, J.14
Munnich, A.15
Melki, J.16
-
19
-
-
0029954338
-
A novel nuclear structure containing the survival of motor neuron protein
-
Liu Q., Dreyfuss G. A novel nuclear structure containing the survival of motor neuron protein. EMBO J. 15:1996;3555-3565.
-
(1996)
EMBO J.
, vol.15
, pp. 3555-3565
-
-
Liu, Q.1
Dreyfuss, G.2
-
20
-
-
0030931727
-
The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins
-
Liu Q., Fischer U., Wang F., Dreyfuss G. The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins. Cell. 90:1997;1013-1021.
-
(1997)
Cell
, vol.90
, pp. 1013-1021
-
-
Liu, Q.1
Fischer, U.2
Wang, F.3
Dreyfuss, G.4
-
21
-
-
0031829338
-
The domain encoded by exon 2 of the survival of motor neuron protein mediates nucleic acid binding
-
Lorson C. L., Androphy E. J. The domain encoded by exon 2 of the survival of motor neuron protein mediates nucleic acid binding. Hum. Mol. Genet. 7:1998;1269-1275.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1269-1275
-
-
Lorson, C.L.1
Androphy, E.J.2
-
22
-
-
0033033434
-
A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy
-
Lorson C. L., Hahnen E., Androphy E. J., Wirth B. A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy. Proc. Natl. Acad. Sci. USA. 96:1999;6307-6311.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 6307-6311
-
-
Lorson, C.L.1
Hahnen, E.2
Androphy, E.J.3
Wirth, B.4
-
23
-
-
0031561729
-
Inhibition of protein dephosphorylation results in the accumulation of splicing snRNPs and coiled bodies within the nucleolus
-
Lyon C. E., Bohmann K., Sleeman J., Lamond A. I. Inhibition of protein dephosphorylation results in the accumulation of splicing snRNPs and coiled bodies within the nucleolus. Exp. Cell Res. 230:1997;84-93.
-
(1997)
Exp. Cell Res.
, vol.230
, pp. 84-93
-
-
Lyon, C.E.1
Bohmann, K.2
Sleeman, J.3
Lamond, A.I.4
-
24
-
-
0033179146
-
Nuclear bodies: Multifaceted subdomains of the interchromatin space
-
Matera A. G. Nuclear bodies: Multifaceted subdomains of the interchromatin space. Trends Cell Biol. 9:1999;302-309.
-
(1999)
Trends Cell Biol.
, vol.9
, pp. 302-309
-
-
Matera, A.G.1
-
26
-
-
0029971161
-
Unusual molecular findings in autosomal recessive spinal muscular atrophy
-
Mattijs G., Schollen E., Legius E., Devriendt K., Goemans N., Kayserili H., Apak M. Y., Cassiman J. J. Unusual molecular findings in autosomal recessive spinal muscular atrophy. J. Med. Genet. 33:1996;469-474.
-
(1996)
J. Med. Genet.
, vol.33
, pp. 469-474
-
-
Mattijs, G.1
Schollen, E.2
Legius, E.3
Devriendt, K.4
Goemans, N.5
Kayserili, H.6
Apak, M.Y.7
Cassiman, J.J.8
-
27
-
-
0030985898
-
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNt and SMNc copy number
-
McAndrew P. E., Parsons D. W., Simard L. R., Rochette C., Ray P. N., Mendell J. R., Prior T., Burghes A. H. M. Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNt and SMNc copy number. Am. J. Hum. Genet. 60:1997;1411-1422.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1411-1422
-
-
McAndrew, P.E.1
Parsons, D.W.2
Simard, L.R.3
Rochette, C.4
Ray, P.N.5
Mendell, J.R.6
Prior, T.7
Burghes, A.H.M.8
-
28
-
-
0031128181
-
Protein phosphorylation and the nuclear organization of pre-mRNA splicing
-
Misteli T., Spector D. L. Protein phosphorylation and the nuclear organization of pre-mRNA splicing. Trends Cell Biol. 7:1997;135-138.
-
(1997)
Trends Cell Biol.
, vol.7
, pp. 135-138
-
-
Misteli, T.1
Spector, D.L.2
-
29
-
-
0032799998
-
A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMA1 from the copy gene SMN2
-
Monani U. R., Lorson C. L., Parsons D. W., Prior T. W., Androphy E. J., Burghes A. H. M., McPherson J. D. A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMA1 from the copy gene SMN2. Hum. Mol. Genet. 8:1999;1177-1183.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1177-1183
-
-
Monani, U.R.1
Lorson, C.L.2
Parsons, D.W.3
Prior, T.W.4
Androphy, E.J.5
Burghes, A.H.M.6
McPherson, J.D.7
-
30
-
-
0027057672
-
Workshop report: International SMA collaboration
-
Munsat T. L., Davies K. E. Workshop report: International SMA collaboration. Neuromusc. Disord. 2:1992;423-428.
-
(1992)
Neuromusc. Disord.
, vol.2
, pp. 423-428
-
-
Munsat, T.L.1
Davies, K.E.2
-
31
-
-
0026355180
-
Localization of the DMDL-gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: Presence at neuromuscular junctions, in the sacrolemma of dystrophic skeletal muscle, in vascular and other smooth muscle and in proliferating brain cell lines
-
thi Man Nguyen, Ellis J. M., Love D. R., Davies K. E., Gatter K. C., Dickson G., Morris G. E. Localization of the DMDL-gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: Presence at neuromuscular junctions, in the sacrolemma of dystrophic skeletal muscle, in vascular and other smooth muscle and in proliferating brain cell lines. J. Cell Biol. 115:1991;1695-1700.
-
(1991)
J. Cell Biol.
, vol.115
, pp. 1695-1700
-
-
Thi Man, N.1
Ellis, J.M.2
Love, D.R.3
Davies, K.E.4
Gatter, K.C.5
Dickson, G.6
Morris, G.E.7
-
32
-
-
0030330044
-
Production of panels of monoclonal antibodies by the hybridoma method
-
G. E. Morris. Totowa: Humana Press
-
thi Man Nguyen, Morris G. E. Production of panels of monoclonal antibodies by the hybridoma method. Morris G. E. Epitope Mapping Protocols. 1996;377-389 Humana Press, Totowa.
-
(1996)
Epitope Mapping Protocols
, pp. 377-389
-
-
Thi Man, N.1
Morris, G.E.2
-
33
-
-
0032567036
-
A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing
-
Pellizzoni L., Kataoka N., Charroux B., Dreyfuss G. A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing. Cell. 95:1998;615-624.
-
(1998)
Cell
, vol.95
, pp. 615-624
-
-
Pellizzoni, L.1
Kataoka, N.2
Charroux, B.3
Dreyfuss, G.4
-
34
-
-
0029827514
-
An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: Further evidence for SMN as the primary SMA-determining gene
-
Parsons D., McAndrew P. E., Monani U. R., Mendell J. R., Burghes A. H. M., Prior T. W. An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene. Hum. Mol. Genet. 5:1996;1727-1732.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1727-1732
-
-
Parsons, D.1
McAndrew, P.E.2
Monani, U.R.3
Mendell, J.R.4
Burghes, A.H.M.5
Prior, T.W.6
-
35
-
-
0030589683
-
Ultrastructure of the nucleus in relation to transcription and splicing: Roles of perichromatin fibrils and interchromatin granules
-
Puvion E., Puvion-Dutilleul F. Ultrastructure of the nucleus in relation to transcription and splicing: Roles of perichromatin fibrils and interchromatin granules. Exp. Cell Res. 229:1996;217-225.
-
(1996)
Exp. Cell Res.
, vol.229
, pp. 217-225
-
-
Puvion, E.1
Puvion-Dutilleul, F.2
-
36
-
-
0025873210
-
Immunological and ultrastructural studies of the nuclear coiled body with autoimmune antibodies
-
Raska I., Andrade L. E., Ochs R. L., Chan E. K., Chang C. M., Roos G., Tan E. M. Immunological and ultrastructural studies of the nuclear coiled body with autoimmune antibodies. Exp. Cell Res. 195:1991;27-37.
-
(1991)
Exp. Cell Res.
, vol.195
, pp. 27-37
-
-
Raska, I.1
Andrade, L.E.2
Ochs, R.L.3
Chan, E.K.4
Chang, C.M.5
Roos, G.6
Tan, E.M.7
-
37
-
-
0028905919
-
Deletions in the survival of motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy
-
Rodrigues N. R., Owen N., Talbot K., Ignatius J., Dubowitz V., Davies K. Deletions in the survival of motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy. Hum. Mol. Genet. 4:1995;631-634.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 631-634
-
-
Rodrigues, N.R.1
Owen, N.2
Talbot, K.3
Ignatius, J.4
Dubowitz, V.5
Davies, K.6
-
38
-
-
0031667334
-
Coiled bodies and U2 snRNa genes adjacent to coiled bodies are enriched in factors required for snRNA transcription
-
Schul E. C., van Driel R., de Jong L. Coiled bodies and U2 snRNa genes adjacent to coiled bodies are enriched in factors required for snRNA transcription. Mol. Biol. Cell. 9:1998;1025-1036.
-
(1998)
Mol. Biol. Cell.
, vol.9
, pp. 1025-1036
-
-
Schul, E.C.1
Van Driel, R.2
De Jong, L.3
-
39
-
-
0030931720
-
Inactivation of the survival of motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos
-
Schrank B., Gotz R., Gunnerson J., Ure J., Toyka K., Smith A., Sendtner M. Inactivation of the survival of motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos. Proc. Natl. Acad. Sci. USA. 94:1997;9920-9925.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 9920-9925
-
-
Schrank, B.1
Gotz, R.2
Gunnerson, J.3
Ure, J.4
Toyka, K.5
Smith, A.6
Sendtner, M.7
-
40
-
-
0033151758
-
Nuclear organisation of pre-mRNA splicing factors
-
Sleeman J. E., Lamond A. I. Nuclear organisation of pre-mRNA splicing factors. Curr. Opin. Cell Biol. 11:1999;372-377.
-
(1999)
Curr. Opin. Cell Biol.
, vol.11
, pp. 372-377
-
-
Sleeman, J.E.1
Lamond, A.I.2
-
41
-
-
0032531261
-
Dynamic interactions between splicing snRNPs, coiled bodies and nucleoli revealed using snRNP protein fusions to the green fluorescent protein
-
Sleeman J., Lyon C. E., Platani M., Kreivi J. P., Lamond A. I. Dynamic interactions between splicing snRNPs, coiled bodies and nucleoli revealed using snRNP protein fusions to the green fluorescent protein. Exp. Cell Res. 243:1998;290-304.
-
(1998)
Exp. Cell Res.
, vol.243
, pp. 290-304
-
-
Sleeman, J.1
Lyon, C.E.2
Platani, M.3
Kreivi, J.P.4
Lamond, A.I.5
-
42
-
-
0031044279
-
-
Talbot K., Ponting C. P., Theodosiou A. M., Rodrigues N. R., Surtees R., Mountford R., Davies K. E. Hum. Mol. Genet. 6:1997;497-500.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 497-500
-
-
Talbot, K.1
Ponting, C.P.2
Theodosiou, A.M.3
Rodrigues, N.R.4
Surtees, R.5
Mountford, R.6
Davies, K.E.7
-
43
-
-
0029819241
-
Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5
-
Van der Steege G., Grootscholten P. M., Cobben J. M., Zappata S., Scheffer H., den Dunnen J. T., van Ommen G. B., Brache C., Buys C. H. C. M. Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5. Am. J. Hum. Genet. 59:1996;834-838.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 834-838
-
-
Van Der Steege, G.1
Grootscholten, P.M.2
Cobben, J.M.3
Zappata, S.4
Scheffer, H.5
Den Dunnen, J.T.6
Van Ommen, G.B.7
Brache, C.8
Buys, C.H.C.M.9
-
44
-
-
0029117950
-
Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: Association of marker genotype with disease severity and candidate cDNAs
-
Wirth B., Hahnen E., Morgan K., DiDonato C. J., Dodze A., Rudnik-Schoneborn S., Simord L. R. Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: Association of marker genotype with disease severity and candidate cDNAs. Hum. Mol. Genet. 4:1995;1273-1284.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1273-1284
-
-
Wirth, B.1
Hahnen, E.2
Morgan, K.3
Didonato, C.J.4
Dodze, A.5
Rudnik-Schoneborn, S.6
Simord, L.R.7
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