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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Detalhes bibliográficos
Autor principal: Anney, R (author)
Outros Autores: Klein, L (author), Pinto, D (author), Pegan, R (author), Magalhães, TR (author), Almeida, J (author), Oliveira, G (author)
Formato: article
Idioma:eng
Publicado em: 2012
Assuntos:
Alelos
Perturbação Autística
Texto completo:http://hdl.handle.net/10400.4/1379
País:Portugal
Oai:oai:rihuc.huc.min-saude.pt:10400.4/1379

Texto Completo

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

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