Loss of the Intellectual Disability and Autism Gene Cc2d1a and Its Homolog Cc2d1b Differentially Affect Spatial Memory, Anxiety, and Hyperactivity

Hundreds of genes are mutated in non-syndromic intellectual disability (ID) and autism spectrum disorder (ASD), with each gene often involved in only a handful of cases. Such heterogeneity can be daunting, but rare recessive loss of function (LOF) mutations can be a good starting point to provide in...

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Detalles Bibliográficos
Autores principales: Zamarbide, Marta, Oaks, Adam W., Pond, Heather L., Adelman, Julia S., Manzini, M. Chiara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840150/
https://www.ncbi.nlm.nih.gov/pubmed/29552027
http://dx.doi.org/10.3389/fgene.2018.00065

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840150/
https://www.ncbi.nlm.nih.gov/pubmed/29552027
http://dx.doi.org/10.3389/fgene.2018.00065

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