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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Detalles Bibliográficos
Autores principales: ZHAO, YUE, CAO, HONG, SONG, YINDI, FENG, YUE, DING, XIAOXUE, PANG, MINGJIE, ZHANG, YUNMEI, ZHANG, HONG, DING, JIAHUAN, XIA, XUESHAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867886/
https://www.ncbi.nlm.nih.gov/pubmed/27082122
http://dx.doi.org/10.3892/ijmm.2016.2565

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867886/
https://www.ncbi.nlm.nih.gov/pubmed/27082122
http://dx.doi.org/10.3892/ijmm.2016.2565

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