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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...
Autores principales: | Zamarbide, Marta, Oaks, Adam W., Pond, Heather L., Adelman, Julia S., Manzini, M. Chiara |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
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 |
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