Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.

We demonstrate that familial hypertrophic cardiomyopathy (FHC), an autosomal dominant disorder of heart muscle, is a genetically heterogeneous disease. The locus responsible for FHC in members of one large kindred was recently mapped to chromosome 14q11-12 (FHC-1). We have characterized three additi...

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發表在:	J Clin Invest
Principais autores:	Solomon, S D, Jarcho, J A, McKenna, W, Geisterfer-Lowrance, A, Germain, R, Salerni, R, Seidman, J G, Seidman, C E
格式:	Artigo
語言:	Inglês
出版:	American Society for Clinical Investigation 1990
主題:	Research Article
在線閱讀:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296820/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1975599/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI114802
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