No Association Between Single Nucleotide Polymorphisms in Distal-Less Homeobox-6 (DLX6) and Autism Spectrum Disorders (ASD) from the Korean Male Population.
- Author:
Hyoun Geun KIM
1
;
SeongSik WON
;
Seung Ku LEE
;
Min NAM
;
Hee Jung BANG
;
Hyun Jung PARK
;
Jin Young YOON
;
Kyung Sik CHOI
;
Mee Sook HONG
;
Joo Ho CHUNG
;
Kyu Bum KWACK
Author Information
1. Medical Genomics Lab, CHA Research Institute, CHA University, Seongnam, Korea. kbkwack@cha.ac.kr, kbkwack@gmail.com
- Publication Type:Original Article
- Keywords:
Autism Spectrum Disorders;
ASD;
DLX6;
SNP
- MeSH:
Autistic Disorder;
Child;
Autism Spectrum Disorder;
DNA;
Gene Expression;
Genotype;
Humans;
Male;
Phenothiazines;
Polymorphism, Single Nucleotide
- From:Journal of the Korean Academy of Child and Adolescent Psychiatry
2010;21(1):17-22
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVES: Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is characterized by abnormalities of social functioning, communication and behavior. The association of the 7q21-34 region with ASD has been reported. The DLX6 gene, which is located at the 7q22 region, is one of the positional and functional candidate genes for ASD. We found that there is no association between DLX6 polymorphisms and ASD in the Korean male population. METHODS: We selected three single nucleotide polymorphisms (SNPs) that might be implicated in the change of the DLX6 gene expression. The genomic DNA was collected from the venous blood of 147 male controls and 179 male patients with ASD. The genotypes of the selected SNPs were determined using the Illumina GoldenGate assay, and the statistical analyses were performed using HapAnalyzer software and SAS Enterprise. RESULTS: We found no association of the three SNPs in the DLX6 gene with ASD in the Korean male population. CONCLUSION: Our study suggests that the three SNPs in the DLX6 gene are not associated with ASD, and we need to analyze the previously reported regions for their associations with ASD.
