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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and PRRX1[original query]
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
Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential.
Circulation. Cardiovascular genetics 2017 Oct 10 (5): .
Tucker Nathan R, Dolmatova Elena V, Lin Honghuang, Cooper Rebecca R, Ye Jiangchuan, Hucker William J, Jameson Heather S, Parsons Victoria A, Weng Lu-Chen, Mills Robert W, Sinner Moritz F, Imakaev Maxim, Leyton-Mange Jordan, Vlahakes Gus, Benjamin Emelia J, Lunetta Kathryn L, Lubitz Steven A, Mirny Leonid, Milan David J, Ellinor Patrick
Genetic Variants Associated With Susceptibility to Atrial Fibrillation in a Japanese Population.
The Canadian journal of cardiology 2016 Nov .
Liu Lian, Ebana Yusuke, Nitta Jun-Ichi, Takahashi Yoshihide, Miyazaki Shinsuke, Tanaka Toshihiro, Komura Masatoshi, Isobe Mitsuaki, Furukawa Tetsus
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