A case of long QT syndrome with atypical clinical phenotype caused by KCNQ1-R555C missense mutation.
- Author:
Guang Qiang WANG
1
;
Yan Yan JING
1
;
Hong Xia CHU
1
;
Wei Feng LIU
1
;
Lin ZHONG
1
Author Information
- Publication Type:Journal Article
- MeSH: Humans; Mutation, Missense; KCNQ1 Potassium Channel/genetics*; Long QT Syndrome/genetics*; Phenotype; Mutation; Pedigree
- From: Chinese Journal of Cardiology 2023;51(8):870-872
- CountryChina
- Language:Chinese
