A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect

The SCN5A mutations have been associated with a variety of arrhythmic disorders, including type 3 long QT syndrome (LQT3), Brugada syndrome and inherited cardiac conduction defects. The relationship between genotype and phenotype in SCN5A mutations is complex. Some SCN5A mutations may cause death or...

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Detalhes bibliográficos
Main Authors: Niu, Dau‐Ming, Hwang, Betau, Hwang, Han‐Wei, Wang, Nana H, Wu, Jer‐Yuarn, Lee, Pi‐Chang, Chien, Jen‐Chung, Shieh, Ru‐Chi
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2006
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2563172/
https://ncbi.nlm.nih.gov/pubmed/16707561
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2006.042192
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