Gene Detection of GPD1-L and the Association with Sudden Unexplained Death Syndrome in Young Adults
10.3969/j.issn.1004-5619.2013.05.008
- VernacularTitle:GPD1-L基因检测及其与青壮年猝死综合征的相关性
- Author:
Xiaolong XU
;
Wen WANG
;
Chao LIU
;
Yiding HOU
;
Lei HUANG
;
Changhui LIU
;
Yue LI
;
Jianding CHENG
- Publication Type:Journal Article
- Keywords:
forensic genetics;
sudden manhood death syndrome;
glycerol-3-phosphate dehydrogenase 1 like gene
- From:
Journal of Forensic Medicine
2013;(5):348-352
- CountryChina
- Language:Chinese
-
Abstract:
Objective To analyze the variations of glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) and address the association with sudden m anhood death syndrom e (SMDS). Methods The genom ic DNA was extracted from blood sam ples of the SMDS group and the norm alcontrolgroup.The exons, exon-in-tron boundaries and 3′-U TRs of coding region of GPD1-L w ere PCRam plified and DNAsequenced di-rectly to confirm the types of variations. The genotype frequency and allele frequency w ere analyzed statistically. Results There w ere tw ovariants in the SMDS group, c.465C>Tand c.*18G>T, the latter existed certain degree difference of genotype distribution and allele frequency betw een the SMDS group and the control group, but there was no statistically significant (P>0.05). Conclusion The relation be-tw een gene m utation of GPD1-L and the occurrence of Chinese SMDS deserves a further research.