Identification of candidate intergenic risk loci in autism spectrum disorder

BACKGROUND: Copy number variations (CNVs) and DNA sequence alterations affecting specific neuronal genes are established risk factors for Autism Spectrum Disorder (ASD). In what is largely considered a genetic condition, so far, these mutations account for ~20% of individuals having an ASD diagnosis...

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Detalles Bibliográficos
Autores principales: Walker, Susan, Scherer, Stephen W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734099/
https://www.ncbi.nlm.nih.gov/pubmed/23879678
http://dx.doi.org/10.1186/1471-2164-14-499

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