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2009 3
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Page 1
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: qiu xb. 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.
HAND2 loss-of-function mutation causes familial dilated cardiomyopathy.
Liu H, Xu YJ, Li RG, Wang ZS, Zhang M, Qu XK, Qiao Q, Li XM, Di RM, Qiu XB, Yang YQ. Liu H, et al. Among authors: qiu xb. Eur J Med Genet. 2019 Sep;62(9):103540. doi: 10.1016/j.ejmg.2018.09.007. Epub 2018 Sep 12. Eur J Med Genet. 2019. PMID: 30217752
ISL1 loss-of-function variation causes familial atrial fibrillation.
Wu SH, Wang XH, Xu YJ, Gu JN, Yang CX, Qiao Q, Guo XJ, Guo YH, Qiu XB, Jiang WF, Yang YQ. Wu SH, et al. Among authors: qiu xb. Eur J Med Genet. 2020 Nov;63(11):104029. doi: 10.1016/j.ejmg.2020.104029. Epub 2020 Aug 6. Eur J Med Genet. 2020. PMID: 32771629
Discovery of TBX20 as a Novel Gene Underlying Atrial Fibrillation.
Li N, Li YJ, Guo XJ, Wu SH, Jiang WF, Zhang DL, Wang KW, Li L, Sun YM, Xu YJ, Yang YQ, Qiu XB. Li N, et al. Among authors: qiu xb. Biology (Basel). 2023 Aug 30;12(9):1186. doi: 10.3390/biology12091186. Biology (Basel). 2023. PMID: 37759586 Free PMC article.
A SHOX2 loss-of-function mutation underlying familial atrial fibrillation.
Li N, Wang ZS, Wang XH, Xu YJ, Qiao Q, Li XM, Di RM, Guo XJ, Li RG, Zhang M, Qiu XB, Yang YQ. Li N, et al. Among authors: qiu xb. Int J Med Sci. 2018 Oct 20;15(13):1564-1572. doi: 10.7150/ijms.27424. eCollection 2018. Int J Med Sci. 2018. PMID: 30443179 Free PMC article.
65 results