Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders

BACKGROUND: Validating the potential pathogenicity of copy number variants (CNVs) identified in genome-wide studies of autism spectrum disorders (ASD) requires detailed assessment of case/control frequencies, inheritance patterns, clinical correlations, and functional impact. Here, we characterize a...

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Detalhes bibliográficos
Autor principal: Correia, CT (author)
Outros Autores: Conceição, IC (author), Oliveira, B (author), Coelho, J (author), Sousa, I (author), Sequeira, AF (author), Almeida, J (author), Café, C (author), Duque, F (author), Mouga, S (author), Roberts, W (author), Gao, K (author), Lowe, JK (author), Thiruvahindrapuram, B (author), Walker, S (author), Marshall, CR (author), Pinto, D (author), Geschwind, JI (author), Scherer, SW (author), Oliveira, G (author), Vicente, AM (author)
Formato: article
Idioma:eng
Publicado em: 2014
Assuntos:
Perturbação Autística
Anexina A1
Texto completo:http://hdl.handle.net/10400.4/1713
País:Portugal
Oai:oai:rihuc.huc.min-saude.pt:10400.4/1713

Texto Completo

http://hdl.handle.net/10400.4/1713

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