Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy.
Yuan HX, Yan K, Hou DY, Zhang ZY, Wang H, Wang X, Zhang J, Xu XR, Liang YH, Zhao WS, Xu L, Zhang L.
Yuan HX, et al. Among authors: zhao ws.
Medicine (Baltimore). 2017 Aug;96(33):e7727. doi: 10.1097/MD.0000000000007727.
Medicine (Baltimore). 2017.
PMID: 28816949
Free PMC article.