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Familial Amyloid Cardiomyopathy Due to TTR Mutations: An underground Cause of Restrictive Cardiomyopathy

✍ Scribed by Frederick L. Ruberg; Daniel P. Judge; Matthew S. Maurer

Book ID: 116339221
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 44 KB
Volume: 15
Category: Article
ISSN: 1532-8414
DOI: 10.1016/j.cardfail.2009.04.003

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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