Identification of MYLK3 mutations in familial dilated cardiomyopathy

Dilated cardiomyopathy (DCM) is a primary cause of heart failure, life-threatening arrhythmias, and cardiac death. Pathogenic mutations have been identified at the loci of more than 50 genes in approximately 50% of DCM cases, while the etiologies of the remainder have yet to be determined. In this s...

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Detalles Bibliográficos
Autores principales: Tobita, Takashige, Nomura, Seitaro, Morita, Hiroyuki, Ko, Toshiyuki, Fujita, Takanori, Toko, Haruhiro, Uto, Kenta, Hagiwara, Nobuhisa, Aburatani, Hiroyuki, Komuro, Issei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727479/
https://www.ncbi.nlm.nih.gov/pubmed/29235529
http://dx.doi.org/10.1038/s41598-017-17769-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727479/
https://www.ncbi.nlm.nih.gov/pubmed/29235529
http://dx.doi.org/10.1038/s41598-017-17769-1

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