Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Arrhythmia and Prrx1[original query] |
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Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation. Journal of medical genetics 2015 Jan 52 (1): 28-36. Tsai Chia-Ti, Hsieh Chia-Shan, Chang Sheng-Nan, Chuang Eric Y, Juang Jyh-Ming Jimmy, Lin Lian-Yu, Lai Ling-Ping, Hwang Juey-Jen, Chiang Fu-Tien, Lin Jiunn-L |
Pitx2 impairs calcium handling in a dose-dependent manner by modulating Wnt signalling. Cardiovascular research 2015 Aug . Lozano-Velasco Estefanía, Hernández-Torres Francisco, Daimi Houria, Serra Selma A, Herraiz Adela, Hove-Madsen Leif, Aránega Amelia, Franco Die |
Association between ZFHX3 and PRRX1 Polymorphisms and Atrial Fibrillation Susceptibility from Meta-Analysis. International journal of hypertension 2021 12 2021 9423576. Wu Liting, Chu Min, Zhuang Wenfa |
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