Common and rare variants in SCN10A modulate the risk of atrial fibrillation
SCN10A基因的常见和罕见变异会影响房颤的风险。
期刊:Circulation-Cardiovascular Genetics
影响因子:
doi:10.1161/HCG.0000000000000022
Jabbari, Javad; Olesen, Morten S; Yuan, Lei; Nielsen, Jonas B; Liang, Bo; Macri, Vincenzo; Christophersen, Ingrid E; Nielsen, Nikolaj; Sajadieh, Ahmad; Ellinor, Patrick T; Grunnet, Morten; Haunsø, Stig; Holst, Anders G; Svendsen, Jesper H; Jespersen, Thomas