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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Bibliografische gegevens
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1998
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051243/
https://ncbi.nlm.nih.gov/pubmed/9541104
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