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...

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Detalhes bibliográficos
Publicado no:Hum Genome Var
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2015
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Article
Acesso em linha: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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