載入...

A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death

BACKGROUND: Mutations in transcription factor NKX2.5 cause congenital heart disease (CHD). We identified a CHD family with atrial septal defects (ASDs), atrioventricular block, ventricular noncompaction, syncope and sudden death. Our objective is to identify the disease-causing mutation in the CHD f...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Ouyang, Ping, Saarel, Elizabeth, Bai, Ying, Luo, Chunyan, Lv, Qiulun, Xu, Yan, Wang, Fan, Fan, Chun, Younoszai, Adel, Chen, Qiuyun, Tu, Xin, Wang, Qing K.
格式: Artigo
語言:Inglês
出版: 2010
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2998397/
https://ncbi.nlm.nih.gov/pubmed/20932824
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cca.2010.09.035
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!