Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death.
Lin Y, He S, Liao Z, Feng R, Liu R, Peng Y, Yu N, Qi H, Chen J, Huang Z, Lei H, Liu Y, Rao F, Deng C, Xue Y, Zhang G, Zhang B, Yao H, Wu S.
Lin Y, et al.
J Electrocardiol. 2018 Mar-Apr;51(2):309-315. doi: 10.1016/j.jelectrocard.2017.10.002. Epub 2017 Oct 10.
J Electrocardiol. 2018.
PMID: 29132927