Open AccessNext-generation sequencing identifies a novel heterozygous I229T mutation on LMNA associated with familial cardiac conduction disease
Author(s) -
Yuan Gao,
Zhonglin Han,
Xiang Wu,
Rongfang Lan,
Xinlin Zhang,
Wenzhi Shen,
Yu Liu,
Xuehua Liu,
Xi Lan,
Biao Xu,
Wei Xu
Publication year - 2020
Publication title -
medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 148
eISSN - 1536-5964
pISSN - 0025-7974
DOI - 10.1097/md.0000000000021797
Subject(s) - lmna , lamin , genetics , mutant , mutation , gene , medicine , biology