Deleterious Variation in BR Serine/Threonine Kinase 2 Classified a Subtype of Autism

Recently, deleterious variants in the BR serine/threonine kinase 2 (BRSK2) gene have been reported in patients with autism spectrum disorder (ASD), suggesting that BRSK2 is a new high-confidence ASD risk gene, which presents an opportunity to understand the underlying neuropathological mechanisms of...

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Detalles Bibliográficos
Autores principales: Deng, Jingxin, Wang, Yi, Hu, Meixin, Lin, Jia, Li, Qiang, Liu, Chunxue, Xu, Xiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Molecular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231588/
https://www.ncbi.nlm.nih.gov/pubmed/35754711
http://dx.doi.org/10.3389/fnmol.2022.904935

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231588/
https://www.ncbi.nlm.nih.gov/pubmed/35754711
http://dx.doi.org/10.3389/fnmol.2022.904935

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