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PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation.
Guo XJ, Qiu XB, Wang J, Guo YH, Yang CX, Li L, Gao RF, Ke ZP, Di RM, Sun YM, Xu YJ, Yang YQ. Guo XJ, et al. Among authors: li l. J Am Heart Assoc. 2021 Dec 7;10(23):e023517. doi: 10.1161/JAHA.121.023517. Epub 2021 Nov 30. J Am Heart Assoc. 2021. PMID: 34845933 Free PMC article.
GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.
Li RG, Xu YJ, Wang J, Liu XY, Yuan F, Huang RT, Xue S, Li L, Liu H, Li YJ, Qu XK, Shi HY, Zhang M, Qiu XB, Yang YQ. Li RG, et al. Among authors: li yj, li l. Am J Cardiol. 2018 Feb 15;121(4):469-474. doi: 10.1016/j.amjcard.2017.11.012. Epub 2017 Nov 23. Am J Cardiol. 2018. PMID: 29325903
ISL1 loss-of-function mutation contributes to congenital heart defects.
Ma L, Wang J, Li L, Qiao Q, Di RM, Li XM, Xu YJ, Zhang M, Li RG, Qiu XB, Li X, Yang YQ. Ma L, et al. Among authors: li x, li xm, li rg, li l. Heart Vessels. 2019 Apr;34(4):658-668. doi: 10.1007/s00380-018-1289-z. Epub 2018 Nov 2. Heart Vessels. 2019. PMID: 30390123
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