Characterization of a novel SCN5A mutation associated with long QT syndrome and arrhythmogenic right ventricular cardiomyopathy in a family.
Li R, Zheng D, Lin C, Chen Y, Bai Y, Zhou N, Zhao Q, Wei W, Wu Q, Deng J, Zhao S, Yao H, Tang S, Luo B, Liu S, Quan L, Liu X, Cheng J, Huang E.
Li R, et al. Among authors: bai y.
Forensic Sci Med Pathol. 2024 Aug 12. doi: 10.1007/s12024-024-00863-y. Online ahead of print.
Forensic Sci Med Pathol. 2024.
PMID: 39133258