| Literature DB >> 32144606 |
Yan Li1, Shuang Qiu1, Weijing Zhong2, Yong Li1, Yunkai Liu3, Yi Cheng4, Yawen Liu5.
Abstract
Autism spectrum disorder (ASD) represents a group of childhood-onset lifelong neuro-developmental disorders. However, the association between single nucleotide polymorphisms (SNPs) in the deleted in colorectal carcinoma (DCC) gene and ASD susceptibility remains unclear. We investigated the association between ASD susceptibility and seven SNPs in DCC on the basis of a case-control study (231 ASD cases and 242 controls) in Chinese Han. We found that there was no association between ASD susceptibility and the seven SNPs in DCC; however, T-A haplotype (rs2229082-rs2270954), T-A-T-C haplotype (rs2229082-rs2270954-rs2292043-rs2292044), C-G-T-C-T haplotype (rs934345-rs17753970-rs2229082-rs2270954-rs2292043), C-G-T-C-T-G haplotype (rs934345-rs17753970-rs2229082-rs2270954-rs2292043-rs2292044), and G-G-T-C-C-C-C haplotype (rs934345-rs17753970-rs2229082-rs2270954-rs2292043-rs2292044-rs16956878) were associated with ASD susceptibility. Our results indicate that the haplotypes formed on the basis of the seven SNPs in DCC may be implicated in ASD.Entities:
Keywords: Autism spectrum disorder; Deleted in colorectal carcinoma gene; Haplotype analysis; Single nucleotide polymorphisms; Susceptibility
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Year: 2020 PMID: 32144606 DOI: 10.1007/s10803-020-04417-3
Source DB: PubMed Journal: J Autism Dev Disord ISSN: 0162-3257