Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy.

Three novel beta cardiac myosin heavy chain (MHC) gene missense mutations, Phe513Cys, Gly716Arg, and Arg719Trp, which cause familial hypertrophic cardiomyopathy (FHC) are described. One mutation in exon 15 (Phe513Cys) does not alter the charge of the encoded amino acid, and affected family members h...

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Detaylı Bibliyografya
Asıl Yazarlar: Anan, R, Greve, G, Thierfelder, L, Watkins, H, McKenna, W J, Solomon, S, Vecchio, C, Shono, H, Nakao, S, Tanaka, H
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1994
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC293763/
https://ncbi.nlm.nih.gov/pubmed/8282798
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