A Mouse Mutation That Dysregulates Neighboring Galnt17 and Auts2 Genes Is Associated with Phenotypes Related to the Human AUTS2 Syndrome

AUTS2 was originally discovered as the gene disrupted by a translocation in human twins with Autism spectrum disorder, intellectual disability, and epilepsy. Since that initial finding, AUTS2-linked mutations and variants have been associated with a very broad array of neuropsychiatric disorders, su...

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Detalles Bibliográficos
Autores principales: Weisner, P. Anne, Chen, Chih-Ying, Sun, Younguk, Yoo, Jennifer, Kao, Wei-Chun, Zhang, Huimin, Baltz, Emily T., Troy, Joseph M., Stubbs, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2019
Materias:
Investigations
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829118/
https://www.ncbi.nlm.nih.gov/pubmed/31554716
http://dx.doi.org/10.1534/g3.119.400723

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829118/
https://www.ncbi.nlm.nih.gov/pubmed/31554716
http://dx.doi.org/10.1534/g3.119.400723

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