Functional Annotation of Genes Overlapping Copy Number Variants in Autistic Patients: Focus on Axon Pathfinding

We have used Gene Ontology (GO) and pathway analyses to uncover the common functions associated to the genes overlapping Copy Number Variants (CNVs) in autistic patients. Our source of data were four published studies [1-4]. We first applied a two-step enrichment strategy for autism-specific genes....

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Detalles Bibliográficos
Autores principales: Sbacchi, Silvia, Acquadro, Francesco, Calò, Ignazio, Calì, Francesco, Romano, Valentino
Formato: Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd. 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874223/
https://www.ncbi.nlm.nih.gov/pubmed/20885821
http://dx.doi.org/10.2174/138920210790886880

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2874223/
https://www.ncbi.nlm.nih.gov/pubmed/20885821
http://dx.doi.org/10.2174/138920210790886880

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