Cargando…
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...
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 |
Ejemplares similares
-
High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan
por: Chen, Chia-Hsiang, et al.
Publicado: (2017) -
ADHD-related symptoms and attention profiles in the unaffected siblings of probands with autism spectrum disorder: focus on the subtypes of autism and Asperger’s disorder
por: Chien, Yi-Ling, et al.
Publicado: (2017) -
Altered cingulate structures and the associations with social awareness deficits and CNTNAP2 gene in autism spectrum disorder
por: Chien, Yi-Ling, et al.
Publicado: (2021) -
Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders
por: Chien, Wei-Hsien, et al.
Publicado: (2013) -
Genetic analysis of GABRB3 as a candidate gene of autism spectrum disorders
por: Chen, Chia-Hsiang, et al.
Publicado: (2014)