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A translational exploration of the effects of WNT2 variants on altered cortical structures in autism spectrum disorder

BACKGROUND: Evidence suggests that cortical anatomy may be aytpical in autism spectrum disorder. The wingless-type MMTV integration site family, member 2 (WNT2), a candidate gene for autism spectrum disorder, may regulate cortical development. However, it is unclear whether WNT2 variants are associa...

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Detalles Bibliográficos
Autores principales: Chien, Yi-Ling, Chen, Yu-Chieh, Chiu, Yen-Nan, Tsai, Wen-Che, Gau, Susan Shur-Fen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: CMA Joule Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648347/
https://www.ncbi.nlm.nih.gov/pubmed/34862305
http://dx.doi.org/10.1503/jpn.210022