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TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Zhang XL, Qiu XB, Yuan F, Wang J, Zhao CM, Li RG, Xu L, Xu YJ, Shi HY, Hou XM, Qu XK, Xu YW, Yang YQ. Zhang XL, et al. Among authors: xu l, xu yw, xu yj. Biochem Biophys Res Commun. 2015 Mar 27;459(1):166-71. doi: 10.1016/j.bbrc.2015.02.094. Epub 2015 Feb 26. Biochem Biophys Res Commun. 2015. PMID: 25725155 Free article.
GATA4 loss-of-function mutations underlie familial tetralogy of fallot.
Yang YQ, Gharibeh L, Li RG, Xin YF, Wang J, Liu ZM, Qiu XB, Xu YJ, Xu L, Qu XK, Liu X, Fang WY, Huang RT, Xue S, Nemer G. Yang YQ, et al. Among authors: xu l, xu yj. Hum Mutat. 2013 Dec;34(12):1662-71. doi: 10.1002/humu.22434. Epub 2013 Sep 17. Hum Mutat. 2013. PMID: 24000169
GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy.
Li RG, Li L, Qiu XB, Yuan F, Xu L, Li X, Xu YJ, Jiang WF, Jiang JQ, Liu X, Fang WY, Zhang M, Peng LY, Qu XK, Yang YQ. Li RG, et al. Among authors: xu l, xu yj. Biochem Biophys Res Commun. 2013 Oct 4;439(4):591-6. doi: 10.1016/j.bbrc.2013.09.023. Epub 2013 Sep 13. Biochem Biophys Res Commun. 2013. PMID: 24041700 Free article.
Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.
Yu H, Xu JH, Song HM, Zhao L, Xu WJ, Wang J, Li RG, Xu L, Jiang WF, Qiu XB, Jiang JQ, Qu XK, Liu X, Fang WY, Jiang JF, Yang YQ. Yu H, et al. Among authors: xu jh, xu l, xu wj. Int J Med Sci. 2014 Apr 7;11(6):554-63. doi: 10.7150/ijms.8407. eCollection 2014. Int J Med Sci. 2014. PMID: 24782644 Free PMC article.
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