A genome-wide scan for common alleles affecting risk for autism

Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify common risk variation, the Autism Genome Project (AGP) Consortium genotyped 1558 rigorously defined ASD fa...

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Bibliographic Details
Main Author: Anney, R (author)
Other Authors: Klein, L (author), Pinto, D (author), Pegan, R (author), Magalhães, TR (author), Almeida, J (author), Oliveira, G (author)
Format: article
Language:eng
Published: 2012
Subjects:
Alelos
Perturbação Autística
Online Access:http://hdl.handle.net/10400.4/1379
Country:Portugal
Oai:oai:rihuc.huc.min-saude.pt:10400.4/1379

Internet

http://hdl.handle.net/10400.4/1379

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