Molecular pathology of familial hypertrophic cardiomyopathy caused by mutations in the cardiac myosin binding protein C gene.

DNA studies in familial hypertrophic cardiomyopathy (FHC) have shown that it is caused by mutations in genes coding for proteins which make up the muscle sarcomere. The majority of mutations in the FHC genes result from missense changes, although one of the most recent genes to be identified (cardia...

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Detalhes bibliográficos
Main Authors: Yu, B, French, J A, Carrier, L, Jeremy, R W, McTaggart, D R, Nicholson, M R, Hambly, B, Semsarian, C, Richmond, D R, Schwartz, K, Trent, R J
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051243/
https://ncbi.nlm.nih.gov/pubmed/9541104
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