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GATA5 loss-of-function mutation in familial dilated cardiomyopathy.
Zhang XL, Dai N, Tang K, Chen YQ, Chen W, Wang J, Zhao CM, Yuan F, Qiu XB, Qu XK, Yang YQ, Xu YW. Zhang XL, et al. Among authors: wang j. Int J Mol Med. 2015 Mar;35(3):763-70. doi: 10.3892/ijmm.2014.2050. Epub 2014 Dec 29. Int J Mol Med. 2015. PMID: 25543888
GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.
Shi LM, Tao JW, Qiu XB, Wang J, Yuan F, Xu L, Liu H, Li RG, Xu YJ, Wang Q, Zheng HZ, Li X, Wang XZ, Zhang M, Qu XK, Yang YQ. Shi LM, et al. Among authors: wang j, wang xz, wang q. Int J Mol Med. 2014 May;33(5):1219-26. doi: 10.3892/ijmm.2014.1700. Epub 2014 Mar 14. Int J Mol Med. 2014. PMID: 24638895
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: wang j. 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.
CASZ1 loss-of-function mutation associated with congenital heart disease.
Huang RT, Xue S, Wang J, Gu JY, Xu JH, Li YJ, Li N, Yang XX, Liu H, Zhang XD, Qu XK, Xu YJ, Qiu XB, Li RG, Yang YQ. Huang RT, et al. Among authors: wang j. Gene. 2016 Dec 20;595(1):62-68. doi: 10.1016/j.gene.2016.09.044. Epub 2016 Sep 28. Gene. 2016. PMID: 27693370 Clinical Trial.
202,715 results
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