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...
Autor principal: | |
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Outros Autores: | , , , , , |
Formato: | conferenceObject |
Idioma: | eng |
Publicado em: |
2016
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Assuntos: | |
Texto completo: | http://hdl.handle.net/10400.18/3521 |
País: | Portugal |
Oai: | oai:repositorio.insa.pt:10400.18/3521 |