Role of a circadian-relevant gene NR1D1 in brain development: possible involvement in the pathophysiology of autism spectrum disorders

In our previous study, we screened autism spectrum disorder (ASD) patients with and without sleep disorders for mutations in the coding regions of circadian-relevant genes, and detected mutations in several clock genes including NR1D1. Here, we further screened ASD patients for NR1D1 mutations and i...

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Detalles Bibliográficos
Autores principales: Goto, Masahide, Mizuno, Makoto, Matsumoto, Ayumi, Yang, Zhiliang, Jimbo, Eriko F., Tabata, Hidenori, Yamagata, Takanori, Nagata, Koh-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338261/
https://www.ncbi.nlm.nih.gov/pubmed/28262759
http://dx.doi.org/10.1038/srep43945

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338261/
https://www.ncbi.nlm.nih.gov/pubmed/28262759
http://dx.doi.org/10.1038/srep43945

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