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Prioritization of Copy Number Variation Loci Associated with Autism from AutDB–An Integrative Multi-Study Genetic Database

Copy number variants (CNVs) are thought to play an important role in the predisposition to autism spectrum disorder (ASD). However, their relatively low frequency and widespread genomic distribution complicates their accurate characterization and utilization for clinical genetics purposes. Here we p...

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Detalhes bibliográficos
Main Authors: Menashe, Idan, Larsen, Eric C., Banerjee-Basu, Sharmila
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3688962/
https://ncbi.nlm.nih.gov/pubmed/23825557
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0066707
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