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TBX1 loss-of-function mutation contributes to congenital conotruncal defects.
Zhang M, Li FX, Liu XY, Hou JY, Ni SH, Wang J, Zhao CM, Zhang W, Kong Y, Huang RT, Xue S, Yang YQ. Zhang M, et al. Among authors: wang j. Exp Ther Med. 2018 Jan;15(1):447-453. doi: 10.3892/etm.2017.5362. Epub 2017 Oct 24. Exp Ther Med. 2018. PMID: 29250159 Free PMC article.
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
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
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