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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: gao 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.
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population.
Li C, Wang F, Yang Y, Fu F, Xu C, Shi L, Li S, Xia Y, Wu G, Cheng X, Liu H, Wang C, Wang P, Hao J, Ke Y, Zhao Y, Liu M, Zhang R, Gao L, Yu B, Zeng Q, Liao Y, Yang B, Tu X, Wang QK. Li C, et al. Among authors: gao l. Hum Genet. 2011 Mar;129(3):239-46. doi: 10.1007/s00439-010-0912-6. Epub 2010 Nov 25. Hum Genet. 2011. PMID: 21107608 Free PMC article.
Acquired long QT syndrome in hospitalized patients.
Yu H, Zhang L, Liu J, Liu Y, Kowey PR, Zhang Y, Chen Y, Wei Y, Gao L, Li H, Du J, Xia Y. Yu H, et al. Among authors: gao l. Heart Rhythm. 2017 Jul;14(7):974-978. doi: 10.1016/j.hrthm.2017.03.014. Epub 2017 Mar 18. Heart Rhythm. 2017. PMID: 28323171
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