KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome.
- Author:
Qian-hao ZHAO
1
;
Chao LIU
;
Long-wu LU
;
Guo-li LÜ
;
Hong LIU
;
Shuang-bo TANG
;
Li QUAN
;
Jian-ding CHENG
Author Information
1. Department of Forensic Pathology, Zhongshan Medical College, Sun Yat-sen University, Guangzhou 510080, China. spongezhao@163.com
- Publication Type:Journal Article
- MeSH:
Base Sequence;
Case-Control Studies;
China;
DNA Mutational Analysis;
Death, Sudden/ethnology*;
ERG1 Potassium Channel;
Ether-A-Go-Go Potassium Channels/genetics*;
Humans;
KCNQ1 Potassium Channel/genetics*;
Long QT Syndrome;
Mutation;
Polymorphism, Single Nucleotide;
Potassium Channels;
Potassium Channels, Voltage-Gated/genetics*
- From:
Journal of Forensic Medicine
2012;28(5):337-346
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate KCNQ1, KCNH2, KCNE1 and KCNE2 gene variants in the cases of sudden manhood death syndrome (SMDS).
METHODS:One hundred and sixteen sporadic cases of SMDS and one hundred and twenty-five healthy controlled samples were enrolled. Genomic DNA was extracted from blood samples. Gene variants of KCNQ1, KCNH2, KCNE1 and KCNE2 were screened by direct sequencing.
RESULTS:A total of 14 mutations and 14 SNP were detected. Two non-synonymous mutations of them were newfound. There was no non-synonymous mutation found in the control group.
CONCLUSION:There are KCNQ1, KCNH2, KCNE1 and KCNE2 gene variants found in Chinese SMDS cases. KCNQ1, KCNH2, KCNE1 and KCNE2 gene mutation may correlate partly with the occurrence of some cases of the SMDS in China.
