Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel

Chen, J; Li, H; Guo, SC; Yang, Z; Sun, SP; Zeng, JJ; Gou, HJ; Chen, YC; Wang, F; Lin, YP; Huang, K; Yue, H; Ma, YT; Lin, YB

Yue, H; Ma, YT; Lin, YB (通讯作者)，Guangdong Med Univ, Dongguan Affiliated Hosp 1, Dongguan 523710, Guangdong, Peoples R China.;Lin, YB (通讯作者)，Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Geriatr Inst, Guangdong Cardiovasc Inst, Guangzhou 510080, Guangdong, Peoples R China.;Ma, YT (通讯作者)，Univ Chinese Acad Sci, Coll Life Sci, Beijing 100049, Peoples R China.

ORPHANET JOURNAL OF RARE DISEASES, 2022; 17 (1):

Abstract

Background Brugada syndrome (Brs) and long QT syndrome (LQTs) are the most observed inherited primary arrhythmia syndromes and channelopathies, which ......

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