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Volumn 19, Issue 5, 2003, Pages 377-380

Different expressions of X-linked cardiomyopathy in monozygotic triplets with Becker's dystrophy

Author keywords

Cardiomyopathy; Dystrophin; Genetics

Indexed keywords

DYSTROPHIN;

EID: 0142247169     PISSN: 15695794     EISSN: 18758312     Source Type: Journal    
DOI: 10.1023/A:1025824105194     Document Type: Article
Times cited : (5)

References (8)
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  • 2
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  • 3
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    • Prevalence and characteristics of dystrophin defects in adult male patients with dilated cardiomyopathy
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    • Arbustini, E.1    Diegoli, M.2    Morbini, P.3
  • 4
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    • X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
    • Towbin JA, Hejtmancik Fielding J, Brink P, et al. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation 1993; 87: 1854-1865.
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    • Richardson, P.1    McKenna, W.2    Bristow, M.3
  • 7
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    • Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy
    • Muntoni F, Di Lenarda A, Porcu M, et al. Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy. Heart 1997; 78: 608-612.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.