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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...
Autores principales: | Menashe, Idan, Larsen, Eric C., Banerjee-Basu, Sharmila |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
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 |
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