Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Death and ISL1[original query] |
---|
Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population. Pediatric cardiology 2013 Apr 34 (4): 938-41. Cresci Monica, Vecoli Cecilia, Foffa Ilenia, Pulignani Silvia, Ait-Ali Lamia, Andreassi Maria Graz |
ISL1 loss-of-function variation causes familial atrial fibrillation. European journal of medical genetics 2020 8 63 (11): 104029. Wu Shao-Hui, Wang Xin-Hua, Xu Ying-Jia, Gu Jia-Ning, Yang Chen-Xi, Qiao Qi, Guo Xiao-Juan, Guo Yu-Han, Qiu Xing-Biao, Jiang Wei-Feng, Yang Yi-Qi |
PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation. Journal of the American Heart Association 2021 11 10 (23): e023517. Guo Xiao-Juan, Qiu Xing-Biao, Wang Jun, Guo Yu-Han, Yang Chen-Xi, Li Li, Gao Ri-Feng, Ke Zun-Ping, Di Ruo-Min, Sun Yu-Min, Xu Ying-Jia, Yang Yi-Qi |
Study of variants associated with ventricular septal defects (VSDs) highlights the unique genetic structure of the Pakistani population. Italian journal of pediatrics 2022 7 48 (1): 124. Sarwar Sumbal, Shabana , Tahir Amna, Liaqat Zainab, Naseer Saher, Seme Rani Summeya, Mehmood Sabahat, Shahid Saleem Ullah, Hasnain Shahi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: