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ORIGINAL ARTICLE
Year : 2012  |  Volume : 60  |  Issue : 6  |  Page : 581--584

RELN gene polymorphisms and susceptibility to autism in Chinese Han population

Peichao Tian 
 Department of Pediatrics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, People’s Republic of China, China

Correspondence Address:
Peichao Tian
Department of Pediatrics, The First Affiliated Hospital of Zhengzhou University, No.1 Jianshe East Road, Zhengzhou
China

Background: Single nucleotide polymorphisms (SNPs) in the Reelin gene (RELN) are likely candidates to confer risk for autism. The objective of the present study is to investigate the association of RELN gene SNPs with autism. Materials and Methods: A total of 367 Chinese Han subjects were recruited, including 186 autism patients and 181 unrelated healthy controls. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and DNA sequencing methods were used to detect RELN gene polymorphisms. The association between SNPs and autism was analyzed in this study. Results: The g.333509A>C in intron12 and g.504742G>A in exon60 were detected in the RELN gene and a significant association was found between the g.504742G>A polymorphism and autism. Allele and genotype frequencies for the g.504742G>A polymorphism in autistic patients were significantly different for healthy subjects. There was no significantly difference in g.333509A>C polymorphism and autism in the studied populations. Conclusions: Our findings indicated that g.333509A>C was not significantly associated with autism. The g.504742G>A polymorphic variant in the RELN gene might affect subjects susceptibility toward autism in Chinese Han population.


How to cite this article:
Tian P. RELN gene polymorphisms and susceptibility to autism in Chinese Han population.Neurol India 2012;60:581-584


How to cite this URL:
Tian P. RELN gene polymorphisms and susceptibility to autism in Chinese Han population. Neurol India [serial online] 2012 [cited 2021 Jan 23 ];60:581-584
Available from: https://www.neurologyindia.com/article.asp?issn=0028-3886;year=2012;volume=60;issue=6;spage=581;epage=584;aulast=Tian;type=0