Association of 25 bp Deletion in MYBPC3 Gene with Left Ventricle Dysfunction in Coronary Artery Disease Patients

RATIONALE: Mutations in MYBPC3 encoding cardiac myosin binding protein C are common genetic cause of hereditary cardiac myopathies. An intronic 25-bp deletion in MYBPC3 at 3′ region is associated with dilated (DCM) and hypertrophic (HCM) cardiomyopathies in Southeast Asia. However, the frequency of...

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Detalles Bibliográficos
Autores principales: Srivastava, Anshika, Garg, Naveen, Mittal, Tulika, Khanna, Roopali, Gupta, Shipra, Seth, Prahlad Kishore, Mittal, Balraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168477/
https://www.ncbi.nlm.nih.gov/pubmed/21915287
http://dx.doi.org/10.1371/journal.pone.0024123

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168477/
https://www.ncbi.nlm.nih.gov/pubmed/21915287
http://dx.doi.org/10.1371/journal.pone.0024123

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