Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals

The oxytocin receptor (OXTR) gene has been implicated as a risk gene for autism spectrum disorder (ASD)—a neurodevelopmental disorder with essential features of impairments in social communication and reciprocal interaction. The genetic associations between common variations in OXTR and ASD have bee...

詳細記述

保存先:
書誌詳細
出版年:Hum Genome Var
主要な著者: Liu, Xiaoxi, Kawashima, Minae, Miyagawa, Taku, Otowa, Takeshi, Latt, Khun Zaw, Thiri, Myo, Nishida, Hisami, Sugiyama, Toshiro, Tsurusaki, Yoshinori, Matsumoto, Naomichi, Mabuchi, Akihiko, Tokunaga, Katsushi, Sasaki, Tsukasa
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group 2015
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4785550/
https://ncbi.nlm.nih.gov/pubmed/27081536
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2015.24
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