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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Detalles Bibliográficos
Autores principales: Menashe, Idan, Larsen, Eric C., Banerjee-Basu, Sharmila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3688962/
https://www.ncbi.nlm.nih.gov/pubmed/23825557
http://dx.doi.org/10.1371/journal.pone.0066707

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3688962/
https://www.ncbi.nlm.nih.gov/pubmed/23825557
http://dx.doi.org/10.1371/journal.pone.0066707

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