Non-synonymous single-nucleotide variations of the human oxytocin receptor gene and autism spectrum disorders: a case–control study in a Japanese population and functional analysis

BACKGROUND: The human oxytocin receptor (hOXTR) is implicated in the etiology of autism spectrum disorders (ASDs) and is a potential target for therapeutic intervention. Several studies have reported single-nucleotide polymorphisms (SNPs) of the OXTR gene associated with ASDs. These SNPs, however, r...

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Detalles Bibliográficos
Autores principales: Ma, Wen-Jie, Hashii, Minako, Munesue, Toshio, Hayashi, Kenshi, Yagi, Kunimasa, Yamagishi, Masakazu, Higashida, Haruhiro, Yokoyama, Shigeru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707786/
https://www.ncbi.nlm.nih.gov/pubmed/23815867
http://dx.doi.org/10.1186/2040-2392-4-22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707786/
https://www.ncbi.nlm.nih.gov/pubmed/23815867
http://dx.doi.org/10.1186/2040-2392-4-22

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