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The development of familial hypertrophic cardiomyopathy: from mutation to bedside

✍ Scribed by Wessel P. Brouwer; Sabine J. van Dijk; Ger J. M. Stienen; Albert C. van Rossum; Jolanda van der Velden; Tjeerd Germans

Book ID: 108714106
Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 301 KB
Volume: 41
Category: Article
ISSN: 0014-2972
DOI: 10.1111/j.1365-2362.2010.02439.x

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## Abstract ## BACKGROUND Nonsyndromic hypertrophic cardiomyopathy (HCM) is a primary cardiac disease transmitted as an autosomal dominant trait. Multiple chromosomal loci have been found to be involved in the etiology of this defect. LEOPARD syndrome is a genetic condition characteristically asso