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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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Autors principals: Menashe, Idan, Larsen, Eric C., Banerjee-Basu, Sharmila
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2013
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Accés en línia: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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