Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Atrial Fibrillation and SHOX2[original query] |
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Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation. Basic research in cardiology 2016 May 111 (3): 36. Hoffmann Sandra, Clauss Sebastian, Berger Ina M, Weiß Birgit, Montalbano Antonino, Röth Ralph, Bucher Madeline, Klier Ina, Wakili Reza, Seitz Hervé, Schulze-Bahr Eric, Katus Hugo A, Flachsbart Friederike, Nebel Almut, Guenther Sabina Pw, Bagaev Erik, Rottbauer Wolfgang, Kääb Stefan, Just Steffen, Rappold Gudrun |
Functional Characterization of Rare Variants in the SHOX2 Gene Identified in Sinus Node Dysfunction and Atrial Fibrillation. Frontiers in genetics 2019 7 10 648. Hoffmann Sandra, Paone Christoph, Sumer Simon A, Diebold Sabrina, Weiss Birgit, Roeth Ralph, Clauss Sebastian, Klier Ina, Kääb Stefan, Schulz Andreas, Wild Philipp S, Ghrib Adil, Zeller Tanja, Schnabel Renate B, Just Steffen, Rappold Gudrun |
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 |
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