Investigation of OLIG2 as a candidate gene for schizophrenia and autism spectrum disorder

A number of genomic mutations that are thought to be strongly involved in the development of schizophrenia (SCZ) and autism spectrum disorder (ASD) have been identified. Abnormalities involving oligodendrocytes have been reported in SCZ, and as a related gene, oligodendrocyte lineage transcription f...

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Detalles Bibliográficos
Autores principales: Furuta, Sho, Aleksic, Branko, Nawa, Yoshihiro, Kimura, Hiroki, Kushima, Itaru, Ishizuka, Kanako, Kato, Hidekazu, Toyama, Miho, Arioka, Yuko, Mori, Daisuke, Morikawa, Mako, Inada, Toshiya, Ozaki, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nagoya University 2022
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350582/
https://www.ncbi.nlm.nih.gov/pubmed/35967956
http://dx.doi.org/10.18999/nagjms.84.2.260

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350582/
https://www.ncbi.nlm.nih.gov/pubmed/35967956
http://dx.doi.org/10.18999/nagjms.84.2.260

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