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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Sci Rep
Prif Awduron: Tobita, Takashige, Nomura, Seitaro, Morita, Hiroyuki, Ko, Toshiyuki, Fujita, Takanori, Toko, Haruhiro, Uto, Kenta, Hagiwara, Nobuhisa, Aburatani, Hiroyuki, Komuro, Issei
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group UK 2017
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5727479/
https://ncbi.nlm.nih.gov/pubmed/29235529
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-17769-1
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