A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve

TBX5 has been linked to Holt-Oram syndrome, with congenital heart defect (CHD) and atrial fibrillation (AF) being two major cardiac phenotypes. However, the prevalence of a TBX5 variation in patients with CHD and AF remains obscure. In this research, by sequencing analysis of TBX5 in 178 index patie...

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שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:Genet Mol Biol
Main Authors: Jiang, Wei-Feng, Xu, Ying-Jia, Zhao, Cui-Mei, Wang, Xin-Hua, Qiu, Xing-Biao, Liu, Xu, Wu, Shao-Hui, Yang, Yi-Qing
פורמט: Artigo
שפה:Inglês
יצא לאור: Sociedade Brasileira de Genética 2020
נושאים:
Human and Medical Genetics
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC7783509/
https://ncbi.nlm.nih.gov/pubmed/33306779
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/1678-4685-GMB-2020-0142
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