Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system

Inherited cardiomyopathy is the major cause of sudden cardiac death (SCD) and heart failure (HF). The disease is associated with extensive genetic heterogeneity; pathogenic mutations in cardiac sarcomere protein genes, cytoskeletal protein genes and nuclear envelope protein genes have been linked to...

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Publicado no:Int J Mol Med
Main Authors: ZHAO, YUE, CAO, HONG, SONG, YINDI, FENG, YUE, DING, XIAOXUE, PANG, MINGJIE, ZHANG, YUNMEI, ZHANG, HONG, DING, JIAHUAN, XIA, XUESHAN
Formato: Artigo
Idioma:Inglês
Publicado em: D.A. Spandidos 2016
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4867886/
https://ncbi.nlm.nih.gov/pubmed/27082122
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ijmm.2016.2565
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