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Genetic heterogeneity of Familial Hypertrophic Cardiomyopathy: Search for a second chromosomal localization

✍ Scribed by L. Carrier; C. Hengstenberg; L. Faure; P. Guicheney; C. Dufour; E. Séboun; M. Komajda; K. Schwartz


Book ID
115985322
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
107 KB
Volume
24
Category
Article
ISSN
0022-2828

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To understand the molecular basis of familial hypertrophic cardiomyopathy (FHC) in the Chinese population, a family with FHC was investigated. Nineteen family members who were 16 years of age or older were examined by M-mode or two-dimensional echocardiography. Eight members were diagnosed to be aff