Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference34 articles.
1. The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy;England;N Engl J Med,1992
2. Frequency of phenotypes of familial dilated cardiomyopathy;Grünig;J Am Coll Cardiol,1998
3. X-linked dilated cardiomyopathy: molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus;Towbin;Circulation,1993
4. Actin mutations in dilated cardiomyopathy: a heritable form of heart failure;Olson;Science,1998
5. Dystrophinopathy, the expanding phenotype-dystrophin abnormalities in X-linked dilated cardiomyopathy;Beggs;Circulation,1997
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