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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785550/
https://www.ncbi.nlm.nih.gov/pubmed/27081536
http://dx.doi.org/10.1038/hgv.2015.24

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785550/
https://www.ncbi.nlm.nih.gov/pubmed/27081536
http://dx.doi.org/10.1038/hgv.2015.24

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