Characterization and expression analysis of a CNV at chromosome 10q22 encompassing 14 genes in an autistic patient

Autism Spectrum Disorders (ASD) have a strong genetic component, with an estimated heritability of over 90%. Recent studies carried out by the Autism Genome Project (AGP) consortium suggest that rare Copy Number Variants (CNV), characterized by submicroscopic chromosomal deletions and duplications,...

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Bibliographic Details
Main Author: C. Conceição, Inês (author)
Other Authors: Correia, Catarina (author), Oliveira, Bárbara (author), Duque, Frederico (author), Mouga, Susana (author), Oliveira, Guiomar (author), M. Vicente, Astrid (author)
Format: conferenceObject
Language:eng
Published: 2012
Subjects:
Perturbações do Desenvolvimento Infantil e Saúde Mental
Online Access:http://hdl.handle.net/10400.18/400
Country:Portugal
Oai:oai:repositorio.insa.pt:10400.18/400

Internet

http://hdl.handle.net/10400.18/400

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