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2014 2
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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: zhao cm. 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 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: zhao cm. 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
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: zhao cm. 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.
19 results