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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Int J Mol Med
Autori principali: ZHAO, YUE, CAO, HONG, SONG, YINDI, FENG, YUE, DING, XIAOXUE, PANG, MINGJIE, ZHANG, YUNMEI, ZHANG, HONG, DING, JIAHUAN, XIA, XUESHAN
Natura: Artigo
Lingua:Inglês
Pubblicazione: D.A. Spandidos 2016
Soggetti:
Articles
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi