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Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy.

BACKGROUND: Familial hypertrophic cardiomyopathy (HCM) is an autosomal dominant disease characterized by ventricular hypertrophy, myocellular disarray, arrhythmias, and sudden death. Mutations in several contractile proteins, including cardiac myosin heavy chains, have been described in families wit...

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Détails bibliographiques
Auteurs principaux: Vikstrom, K. L., Factor, S. M., Leinwand, L. A.
Format: Artigo
Langue:Inglês
Publié: The Feinstein Institute for Medical Research 1996
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2230192/
https://ncbi.nlm.nih.gov/pubmed/8898372
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