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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Detaylı Bibliyografya
Asıl Yazarlar: Solomon, S D, Jarcho, J A, McKenna, W, Geisterfer-Lowrance, A, Germain, R, Salerni, R, Seidman, J G, Seidman, C E
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1990
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC296820/
https://ncbi.nlm.nih.gov/pubmed/1975599
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