메뉴 건너뛰기




Volumn 6, Issue 1, 2013, Pages 65-80

Erratum: Early results of sarcomeric gene screening from the Egyptian national BA-HCM program (Journal of Cardiovascular Translational Research DOI:10.1007/s12265-012-9425-0);Early results of sarcomeric gene screening from the egyptian national BA-HCM program

Author keywords

Egypt; HCM genetics; Sarcomeric genotyping

Indexed keywords

ALANINE; CYSTEINE; GLYCINE; MYOSIN BINDING PROTEIN C; MYOSIN HEAVY CHAIN BETA; THREONINE; TROPONIN T;

EID: 84872612727     PISSN: 19375387     EISSN: 19375395     Source Type: Journal    
DOI: 10.1007/s12265-013-9478-8     Document Type: Erratum
Times cited : (34)

References (52)
  • 1
    • 23044503392 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy in the community: Why we should care
    • DOI 10.1038/ncpcardio0248, PII N0248
    • Cecchi, F; Yacoub, M. H; & Olivotto, I. (2005). Hypertrophic cardiomyopathy in the community: why we should care. Nature Clinical Practice. Cardiovascular Medicine, 2(7), 324-325. (Pubitemid 41670312)
    • (2005) Nature Clinical Practice Cardiovascular Medicine , vol.2 , Issue.7 , pp. 324-325
    • Cecchi, F.1    Yacoub, M.H.2    Olivotto, I.3
  • 2
    • 0029083650 scopus 로고
    • Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults
    • 7641357 10.1161/01.CIR.92.4.785 1:STN:280:DyaK2MzmvVyisg%3D%3D
    • Maron, B. J; Gardin, J. M; Flack, J. M; Gidding, S. S; Kurosaki, T. T; & Bild, D. E. (1995). Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults. Circulation, 92(4), 785-789.
    • (1995) Circulation , vol.92 , Issue.4 , pp. 785-789
    • Maron, B.J.1    Gardin, J.M.2    Flack, J.M.3    Gidding, S.S.4    Kurosaki, T.T.5    Bild, D.E.6
  • 3
    • 0347989434 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy: An important global disease
    • DOI 10.1016/j.amjmed.2003.10.012
    • Maron, B. J. (2004). Hypertrophic cardiomyopathy: an important global disease. American Journal of Medicine, 116(1), 63-65. (Pubitemid 38050032)
    • (2004) American Journal of Medicine , vol.116 , Issue.1 , pp. 63-65
    • Maron, B.J.1
  • 4
    • 58149504202 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy without hypertrophy: An emerging pre-clinical subgroup composed of genetically affected family members
    • 19356535 10.1016/j.jcmg.2008.09.008
    • Maron, B. J; & Ho, C. Y. (2009). Hypertrophic cardiomyopathy without hypertrophy: an emerging pre-clinical subgroup composed of genetically affected family members. JACC. Cardiovascular Imaging, 2(1), 65-68.
    • (2009) JACC. Cardiovascular Imaging , vol.2 , Issue.1 , pp. 65-68
    • Maron, B.J.1    Ho, C.Y.2
  • 5
    • 84872597393 scopus 로고    scopus 로고
    • (accessed July17, 2012)
    • http://www.indexmundi.com/egypt/population.html (accessed July17, 2012).
  • 8
    • 79955519460 scopus 로고    scopus 로고
    • Inherited cardiomyopathy
    • 21524215 10.1056/NEJMra0902923 1:CAS:528:DC%2BC3MXlsFeltLk%3D
    • Watkins, H; Ashrafian, H; & Redwood, C. (2011). Inherited cardiomyopathy. NEJM, 364, 1643-1656.
    • (2011) NEJM , vol.364 , pp. 1643-1656
    • Watkins, H.1    Ashrafian, H.2    Redwood, C.3
  • 9
    • 77954985787 scopus 로고    scopus 로고
    • Heterogeneity of clinical manifestation of hypertrophic cardiomyopathy caused by deletion of lysine 183 in cardiac troponin i gene
    • 20558914 10.1536/ihj.51.214
    • Funada, A; Masuta, E; Fujino, N; Hayashi, K; Ino, H; Kita, Y; Ikeda, H; Fujii, T; Nakanuma, Y; & Yamagishi, M. (2010). Heterogeneity of clinical manifestation of hypertrophic cardiomyopathy caused by deletion of lysine 183 in cardiac troponin I gene. International Heart Journal, 51(3), 214-217.
    • (2010) International Heart Journal , vol.51 , Issue.3 , pp. 214-217
    • Funada, A.1    Masuta, E.2    Fujino, N.3    Hayashi, K.4    Ino, H.5    Kita, Y.6    Ikeda, H.7    Fujii, T.8    Nakanuma, Y.9    Yamagishi, M.10
  • 13
    • 4043081356 scopus 로고    scopus 로고
    • Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy
    • DOI 10.1016/j.jacc.2004.04.039, PII S0735109704009568
    • Van Driest, S. L; Jaeger, M. A; Ommen, S. R; Will, M. L; Gersh, B. J; Tajik, A. J; et al. (2004). Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy. Journal of the American College of Cardiology, 44(3), 602-610. (Pubitemid 39078187)
    • (2004) Journal of the American College of Cardiology , vol.44 , Issue.3 , pp. 602-610
    • Van Driest, S.L.1    Jaeger, M.A.2    Ommen, S.R.3    Will, M.L.4    Gersh, B.J.5    Tajik, A.J.6    Ackerman, M.J.7
  • 14
    • 33748463805 scopus 로고    scopus 로고
    • A molecular screening strategy based on β-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy
    • DOI 10.2459/01.JCM.0000237908.26377.d6, PII 0124466520060800000007
    • Girolami, F; Olivotto, I; Passerini, I; Zachara, E; Nistri, S; Re, F; et al. (2006). A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy. Journal of Cardiovascular Medicine, 7(8), 601-607. (Pubitemid 44350495)
    • (2006) Journal of Cardiovascular Medicine , vol.7 , Issue.8 , pp. 601-607
    • Girolami, F.1    Olivotto, I.2    Passerini, I.3    Zachara, E.4    Nistri, S.5    Re, F.6    Fantini, S.7    Baldini, K.8    Torricelli, F.9    Cecchi, F.10
  • 16
    • 0035719186 scopus 로고    scopus 로고
    • Molecular genetics and pathogenesis of hypertrophic cardiomyopathy
    • Marian, A. J; Salek, L; & Lutucuta, S. (2001). Molecular genetics and pathogenesis of hypertrophic cardiomyopathy. Minerva Medica, 92(6), 435-451. (Pubitemid 34184275)
    • (2001) Minerva Medica , vol.92 , Issue.6 , pp. 435-451
    • Marian, A.J.1    Salek, L.2    Lutucuta, S.3
  • 21
    • 67651031014 scopus 로고    scopus 로고
    • A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy
    • 19659763 10.1111/j.1399-0004.2009.01190.x 1:STN:280: DC%2BD1MrktVSntQ%3D%3D
    • Frisso, G; Limongelli, G; Pacileo, G; Del Giudice, A; Forgione, L; Calabro, P; et al. (2009). A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy. Clinical Genetics, 76(1), 91-101.
    • (2009) Clinical Genetics , vol.76 , Issue.1 , pp. 91-101
    • Frisso, G.1    Limongelli, G.2    Pacileo, G.3    Del Giudice, A.4    Forgione, L.5    Calabro, P.6
  • 22
    • 21844449187 scopus 로고    scopus 로고
    • Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect
    • DOI 10.1016/j.ijcard.2004.05.060, PII S0167527304005339
    • Garcia-Castro, M; Reguero, J. R; Alvarez, V; Batalla, A; Soto, M. I; Albaladejo, V; et al. (2005). Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect. International Journal of Cardiology, 102(3), 501-507. (Pubitemid 40956911)
    • (2005) International Journal of Cardiology , vol.102 , Issue.3 , pp. 501-507
    • Garcia-Castro, M.1    Reguero, J.R.2    Alvarez, V.3    Batalla, A.4    Soto, M.I.5    Albaladejo, V.6    Coto, E.7
  • 24
    • 77956941980 scopus 로고    scopus 로고
    • Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy
    • 20624503 10.1016/j.ejmg.2010.07.007
    • Millat, G; Bouvagnet, P; Chevalier, P; Dauphin, C; Jouk, P. S; Da Costa, A; et al. (2010). Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy. European Journal of Medical Genetics, 53(5), 261-267.
    • (2010) European Journal of Medical Genetics , vol.53 , Issue.5 , pp. 261-267
    • Millat, G.1    Bouvagnet, P.2    Chevalier, P.3    Dauphin, C.4    Jouk, P.S.5    Da Costa, A.6
  • 25
    • 77951549322 scopus 로고    scopus 로고
    • Screening mutations in myosin binding protein C3 gene in a cohort of patients with hypertrophic cardiomyopathy
    • 20433692 10.1186/1471-2350-11-67
    • Rodriguez-Garcia, M. I; Monserrat, L; Ortiz, M; Fernandez, X; Cazon, L; Nunez, L; et al. (2010). Screening mutations in myosin binding protein C3 gene in a cohort of patients with hypertrophic cardiomyopathy. BMC Medical Genetics, 11, 67.
    • (2010) BMC Medical Genetics , vol.11 , pp. 67
    • Rodriguez-Garcia, M.I.1    Monserrat, L.2    Ortiz, M.3    Fernandez, X.4    Cazon, L.5    Nunez, L.6
  • 26
    • 0026409603 scopus 로고
    • Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes
    • 1944483 10.1056/NEJM199112193252501 1:STN:280:DyaK38%2FkvFKgtw%3D%3D
    • Rosenzweig, A; Watkins, H; Hwang, D. S; Miri, M; McKenna, W; Traill, T. A; et al. (1991). Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes. The New England Journal of Medicine, 325(25), 1753-1760.
    • (1991) The New England Journal of Medicine , vol.325 , Issue.25 , pp. 1753-1760
    • Rosenzweig, A.1    Watkins, H.2    Hwang, D.S.3    Miri, M.4    McKenna, W.5    Traill, T.A.6
  • 27
    • 0026573969 scopus 로고
    • Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
    • 1552912 10.1056/NEJM199204233261703 1:STN:280:DyaK383gsVWqsQ%3D%3D
    • Watkins, H; Rosenzweig, A; Hwang, D. S; Levi, T; McKenna, W; Seidman, C. E; et al. (1992). Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. The New England Journal of Medicine, 326(17), 1108-1114.
    • (1992) The New England Journal of Medicine , vol.326 , Issue.17 , pp. 1108-1114
    • Watkins, H.1    Rosenzweig, A.2    Hwang, D.S.3    Levi, T.4    McKenna, W.5    Seidman, C.E.6
  • 29
    • 0007055077 scopus 로고
    • A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy
    • Consevage, M. W; Salada, G. C; Baylen, B. G; Ladda, R. L; & Rogan, P. K. (1994). A new missense mutation, Arg719Gln, in the beta-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy. Human Molecular Genetics, 3(6), 1025-1026. (Pubitemid 24189987)
    • (1994) Human Molecular Genetics , vol.3 , Issue.6 , pp. 1025-1026
    • Consevage, M.W.1    Salada, G.C.2    Baylen, B.G.3    Ladda, R.L.4    Rogan, P.K.5
  • 30
    • 0029047017 scopus 로고
    • Altered actin binding with myosin mutation in hypertrophic cardiomyopathy and sudden death
    • 7739336 10.1016/S0140-6736(95)92034-X 1:STN:280:DyaK2M3lslOjtw%3D%3D
    • Kato, M; Takazawa, K; Kimura, A; Ruegg, J. C; Amano, K; Wang, Y; et al. (1995). Altered actin binding with myosin mutation in hypertrophic cardiomyopathy and sudden death. Lancet, 345(8959), 1247.
    • (1995) Lancet , vol.345 , Issue.8959 , pp. 1247
    • Kato, M.1    Takazawa, K.2    Kimura, A.3    Ruegg, J.C.4    Amano, K.5    Wang, Y.6
  • 31
    • 0029144056 scopus 로고
    • Identification of a novel Ala797Thr mutation in exon 21 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy
    • 10.1002/humu.1380060219
    • Moolman-Smook, J. C; Brink, P. A; & Corfield, V. A. (1995). Identification of a novel Ala797Thr mutation in exon 21 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy. Human Mutation, 6(2), 197-198.
    • (1995) Human Mutation , vol.6 , Issue.2 , pp. 197-198
    • Moolman-Smook, J.C.1    Brink, P.A.2    Corfield, V.A.3
  • 32
    • 18444392736 scopus 로고    scopus 로고
    • Denaturing high performance liquid chromatography: High throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease
    • DOI 10.1136/jcp.2004.021642
    • Yu, B; Sawyer, N. A; Caramins, M; Yuan, Z. G; Saunderson, R. B; Pamphlett, R; et al. (2005). Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease. Journal of Clinical Pathology, 58(5), 479-485. (Pubitemid 40646866)
    • (2005) Journal of Clinical Pathology , vol.58 , Issue.5 , pp. 479-485
    • Yu, B.1    Sawyer, N.A.2    Caramins, M.3    Yuan, Z.G.4    Saunderson, R.B.5    Pamphlett, R.6    Richmond, D.R.7    Jeremy, R.W.8    Trent, R.J.9
  • 33
    • 80051934413 scopus 로고    scopus 로고
    • Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy
    • 21302287 10.1002/jcp.22636 1:CAS:528:DC%2BC3MXhtVKksrbE
    • Roncarati, R; Latronico, M. V; Musumeci, B; Aurino, S; Torella, A; Bang, M. L; et al. (2011). Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy. Journal of Cellular Physiology, 226(11), 2894-2900.
    • (2011) Journal of Cellular Physiology , vol.226 , Issue.11 , pp. 2894-2900
    • Roncarati, R.1    Latronico, M.V.2    Musumeci, B.3    Aurino, S.4    Torella, A.5    Bang, M.L.6
  • 38
    • 0033361790 scopus 로고    scopus 로고
    • The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: A unique profile of both independent and founder events
    • DOI 10.1086/302623
    • Moolman-Smook, J. C; De Lange, W. J; Bruwer, E. C. D; Brink, P. A; & Corfield, V. A. (1999). The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events. American Journal of Human Genetics, 65, 1308-1320. (Pubitemid 30460381)
    • (1999) American Journal of Human Genetics , vol.65 , Issue.5 , pp. 1308-1320
    • Moolman-Smook, J.C.1    De Lange, W.J.2    Bruwer, E.C.D.3    Brink, P.A.4    Corfield, V.A.5
  • 42
    • 0032231701 scopus 로고    scopus 로고
    • Neighboring-nucleotide effects on the rates of germ-line single-base- pair substitution in human genes
    • DOI 10.1086/301965
    • Krawczak, M; Ball, E. V; & Cooper, D. N. (1998). Neighboring- nucleotide effects on the rates of germ-line single-base-pair substitution in human genes. American Journal of Human Genetics, 63(2), 474-488. (Pubitemid 30418629)
    • (1998) American Journal of Human Genetics , vol.63 , Issue.2 , pp. 474-488
    • Krawczak, M.1    Ball, E.V.2    Cooper, D.N.3
  • 44
    • 29644439205 scopus 로고    scopus 로고
    • Cytosine methylation and DNA repair
    • DOI 10.1007/3-540-31390-7-11
    • Walsh, C. P; & Xu, G. L. (2006). Cytosine methylation and DNA repair. Current Topics in Microbiology and Immunology, 301, 283-315. (Pubitemid 43022677)
    • (2006) Current Topics in Microbiology and Immunology , vol.301 , pp. 283-315
    • Walsh, C.P.1    Xu, G.L.2
  • 46
    • 49649083832 scopus 로고    scopus 로고
    • Evaluation of the flanking nucleotide sequences of sarcomeric hypertrophic cardiomyopathy substitution mutations
    • 18539302 10.1016/j.mrfmmm.2008.04.005 1:CAS:528:DC%2BD1cXns1ahs7Y%3D
    • Meurs, K. M; & Mealey, K. L. (2008). Evaluation of the flanking nucleotide sequences of sarcomeric hypertrophic cardiomyopathy substitution mutations. Mutation Research, 642(1-2), 86-89.
    • (2008) Mutation Research , vol.642 , Issue.1-2 , pp. 86-89
    • Meurs, K.M.1    Mealey, K.L.2
  • 49
    • 0033361790 scopus 로고    scopus 로고
    • The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: A unique profile of both independent and founder events
    • DOI 10.1086/302623
    • Moolman-Smook, J. C; De Lange, W. J; Bruwer, E. C. D; Brink, P. A; & Corfield, V. A. (1999). The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events. American Journal of Human Genetics, 65, 1308-1320. (Pubitemid 30460381)
    • (1999) American Journal of Human Genetics , vol.65 , Issue.5 , pp. 1308-1320
    • Moolman-Smook, J.C.1    De Lange, W.J.2    Bruwer, E.C.D.3    Brink, P.A.4    Corfield, V.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.