Effects of heterozygous deletion of autism-related gene Cullin-3 in mice

Autism Spectrum Disorder (ASD) is a developmental disorder in which children display repetitive behavior, restricted range of interests, and atypical social interaction and communication. CUL3, coding for a Cullin family scaffold protein mediating assembly of ubiquitin ligase complexes through BTB d...

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Detalles Bibliográficos
Autores principales: Xia, Qiang-qiang, Walker, Angela K., Song, Chenghui, Wang, Jing, Singh, Anju, Mobley, James A., Xuan, Zhong X., Singer, Jeffrey D., Powell, Craig M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332626/
https://www.ncbi.nlm.nih.gov/pubmed/37428799
http://dx.doi.org/10.1371/journal.pone.0283299

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332626/
https://www.ncbi.nlm.nih.gov/pubmed/37428799
http://dx.doi.org/10.1371/journal.pone.0283299

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