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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: li x, li l. 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.
GATA6 loss-of-function mutation in atrial fibrillation.
Yang YQ, Li L, Wang J, Zhang XL, Li RG, Xu YJ, Tan HW, Wang XH, Jiang JQ, Fang WY, Liu X. Yang YQ, et al. Among authors: li rg, li l. Eur J Med Genet. 2012 Oct;55(10):520-6. doi: 10.1016/j.ejmg.2012.06.007. Epub 2012 Jun 26. Eur J Med Genet. 2012. PMID: 22750565
Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation.
Yang Y, Li J, Lin X, Yang Y, Hong K, Wang L, Liu J, Li L, Yan D, Liang D, Xiao J, Jin H, Wu J, Zhang Y, Chen YH. Yang Y, et al. Among authors: li j, li l. J Hum Genet. 2009 May;54(5):277-83. doi: 10.1038/jhg.2009.26. Epub 2009 Apr 3. J Hum Genet. 2009. PMID: 19343045
Identification of a Kir3.4 mutation in congenital long QT syndrome.
Yang Y, Yang Y, Liang B, Liu J, Li J, Grunnet M, Olesen SP, Rasmussen HB, Ellinor PT, Gao L, Lin X, Li L, Wang L, Xiao J, Liu Y, Liu Y, Zhang S, Liang D, Peng L, Jespersen T, Chen YH. Yang Y, et al. Among authors: li j, li l. Am J Hum Genet. 2010 Jun 11;86(6):872-80. doi: 10.1016/j.ajhg.2010.04.017. Am J Hum Genet. 2010. PMID: 20560207 Free PMC article.
Dynamin-2 mediates heart failure by modulating Ca2+ -dependent cardiomyocyte apoptosis.
Li J, Zhang DS, Ye JC, Li CM, Qi M, Liang DD, Xu XR, Xu L, Liu Y, Zhang H, Zhang YY, Deng FF, Feng J, Shi D, Chen JJ, Li L, Chen G, Sun YF, Peng LY, Chen YH. Li J, et al. Among authors: li l, li cm. Int J Cardiol. 2013 Oct 3;168(3):2109-19. doi: 10.1016/j.ijcard.2013.01.006. Epub 2013 Feb 11. Int J Cardiol. 2013. PMID: 23410488
92,334 results
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