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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Detalles Bibliográficos
Autores principales: 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: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880974/
https://www.ncbi.nlm.nih.gov/pubmed/20433692
http://dx.doi.org/10.1186/1471-2350-11-67

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2880974/
https://www.ncbi.nlm.nih.gov/pubmed/20433692
http://dx.doi.org/10.1186/1471-2350-11-67

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