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Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Hypertrophic cardiomyopathy occurs as an autosomal dominant familial disorder or as a sporadic disease without familial involvement. While missense mutations in the beta cardiac myosin heavy chain (MHC) gene account for approximately half of all cases of familial hypertrophic cardiomyopathy, the mol...

詳細記述

保存先:
書誌詳細
出版年:J Clin Invest
主要な著者: Watkins, H, Thierfelder, L, Hwang, D S, McKenna, W, Seidman, J G, Seidman, C E
フォーマット: Artigo
言語:Inglês
出版事項: American Society for Clinical Investigation 1992
主題:
オンライン・アクセス:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC443222/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1430197/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116038
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