Orientador(es)
Resumo(s)
The main objective of this work is to identify Single Nucleotide Variants (SNVs) that play a role in ASD
etiology in neurotransmission and synaptic genes since there is strong genomic and functional evidence
that these biological processes are altered in ASD.
Descrição
Joana M. Vilela is a fellow of the BioSys PhD Programme and a recipient of a PhD grant, with reference PD/BD/131390/2017, funded by FCT – Fundação para a Ciência e a Tecnologia.
Palavras-chave
Autism Spectrum Disorder Single Nucleotide Variants Autismo Perturbações do Desenvolvimento Infantil e Saúde Mental
Contexto Educativo
Citação
Editora
Instituto Nacional de Saúde Doutor Ricardo Jorge, IP
