Novel Rod Domain Duplication in Dystrophin Resulting in X-Linked Dilated Cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy;Cohen;Heart,2004
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3. The medical genetics of dystrophinopathies: molecular genetic diagnosis and its impact on clinical practice;Ferlini;Neuromuscul Disord,2012
4. Mutation of dystrophin gene and cardiomyopathy;Nigro;Neuromuscul Disord,1994
5. A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy;Bies;J Mol Cell Cardiol,1997
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