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Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles.
Lin Y, Zhang Q, Zhong ZA, Xu Z, He S, Rao F, Liu Y, Tang J, Wang F, Liu H, Xie J, Wu H, Wang S, Li X, Shan Z, Deng C, Liao Z, Deng H, Liao H, Xue Y, Chen W, Zhan X, Zhang B, Wu S. Lin Y, et al. Among authors: zhang b, zhang q. Cardiology. 2017;138(1):41-54. doi: 10.1159/000462962. Epub 2017 Jun 3. Cardiology. 2017. PMID: 28578331
Involvement of Src tyrosine kinase and protein kinase C in the expression of macrophage migration inhibitory factor induced by H2O2 in HL-1 mouse cardiac muscle cells.
Rao F, Deng CY, Zhang QH, Xue YM, Xiao DZ, Kuang SJ, Lin QX, Shan ZX, Liu XY, Zhu JN, Yu XY, Wu SL. Rao F, et al. Among authors: zhang qh. Braz J Med Biol Res. 2013 Sep;46(9):746-51. doi: 10.1590/1414-431X20132936. Epub 2013 Sep 6. Braz J Med Biol Res. 2013. PMID: 24036910 Free PMC article.
Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation.
Lin Y, Huang J, He S, Feng R, Zhong Z, Liu Y, Ye W, Li X, Liao H, Fei H, Rao F, Shan Z, Deng C, Zhan X, Xue Y, Liu H, Zhang B, Wang K, Zhang Q, Wu S, Lin X. Lin Y, et al. Among authors: zhang b, zhang q. BMC Med Genet. 2018 Aug 21;19(1):148. doi: 10.1186/s12881-018-0580-2. BMC Med Genet. 2018. PMID: 30129429 Free PMC article.
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