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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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Zamarbide, Marta, Oaks, Adam W., Pond, Heather L., Adelman, Julia S., Manzini, M. Chiara
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5840150/
https://ncbi.nlm.nih.gov/pubmed/29552027
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00065
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