FGF12 is a candidate Brugada syndrome locus

BACKGROUND: Less than 30% of the cases of Brugada syndrome (BrS) have an identified genetic cause. Of the known BrS-susceptibility genes, loss-of-function mutations in SCN5A or CACNA1C and their auxiliary subunits are most common. On the basis of the recent demonstration that fibroblast growth facto...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Hennessey, Jessica A., Marcou, Cherisse A., Wang, Chuan, Wei, Eric Q., Wang, Chaojian, Tester, David J., Torchio, Margherita, Dagradi, Federica, Crotti, Lia, Schwartz, Peter J., Ackerman, Michael J., Pitt, Geoffrey S.
格式: Artigo
語言:Inglês
出版: 2013
主題:
Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC3870051/
https://ncbi.nlm.nih.gov/pubmed/24096171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2013.09.064
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!

相似書籍