Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy

BACKGROUND: MyBPC3 mutations are amongst the most frequent causes of hypertrophic cardiomyopathy, however, its prevalence varies between populations. They have been associated with mild and late onset disease expression. Our objectives were to establish the prevalence of MyBPC3 mutations and determi...

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Detalhes bibliográficos
Main Authors: Rodríguez-García, María Isabel, Monserrat, Lorenzo, Ortiz, Martín, Fernández, Xusto, Cazón, Laura, Núñez, Lucía, Barriales-Villa, Roberto, Maneiro, Emilia, Veira, Elena, Castro-Beiras, Alfonso, Hermida-Prieto, Manuel
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2880974/
https://ncbi.nlm.nih.gov/pubmed/20433692
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-67
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