Novel Autism Spectrum Disorder (ASD) Risk Genes identified in Genome-Wide Association Studies (GWAS) through Protein Interaction Network analysis

ASD is a common disorder with heterogeneous clinical presentation and unclear etiology. Rare, highly penetrant, variants explain approximately 20% of ASD genetic liability, while common genetic factors of low effect, which combine in affected individuals to reach a pathological threshold, have prove...

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Detalhes bibliográficos
Autor principal: Vicente, A.M. (author)
Outros Autores: Correia, Catarina (author), Conceição, Inês (author), Kwiatkowska, Katarzyna (author), Rodrigues, Catarina (author), Marques, Ana Rita (author), Oliveira, Guiomar (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2016
Assuntos:
Texto completo:http://hdl.handle.net/10400.18/3521
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/3521