Novel Phenotype–Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing

BACKGROUND: MYBPC3 dysfunctions have been proven to induce dilated cardiomyopathy, hypertrophic cardiomyopathy, and/or left ventricular noncompaction; however, the genotype–phenotype correlation between MYBPC3 and restrictive cardiomyopathy (RCM) has not been established. The newly developed next-ge...

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Detalles Bibliográficos
Autores principales: Wu, Wei, Lu, Chao-Xia, Wang, Yi-Ning, Liu, Fang, Chen, Wei, Liu, Yong-Tai, Han, Ye-Chen, Cao, Jian, Zhang, Shu-Yang, Zhang, Xue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608072/
https://www.ncbi.nlm.nih.gov/pubmed/26163040
http://dx.doi.org/10.1161/JAHA.115.001879

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608072/
https://www.ncbi.nlm.nih.gov/pubmed/26163040
http://dx.doi.org/10.1161/JAHA.115.001879

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