Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.

Familial hypertrophic cardiomyopathy (FHC) is a clinically and genetically heterogeneous disease. The first identified disease gene, located on chromosome 14q11-q12, encodes the beta-myosin heavy chain. We have performed linkage analysis of two French FHC pedigrees, 720 and 730, with two microsatell...

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Bibliografiset tiedot

Julkaisussa:	J Clin Invest
Päätekijät:	Dausse, E, Komajda, M, Fetler, L, Dubourg, O, Dufour, C, Carrier, L, Wisnewsky, C, Bercovici, J, Hengstenberg, C, al-Mahdawi, S
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	American Society for Clinical Investigation 1993
Aiheet:	Research Article
Linkit:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC288481/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8254035/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116900
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