miRNA and lncRNA gene variants in Autism Spectrum Disorder

A.R.Marques is recipiente of a fellowship from BioSys PhD programme (Ref PD/BD/113773/2015 from FCT (Portugal). Patients and parents were genotyped in the context of the Autism Genome Project (AGP), funded by NIMH, HRB, MRC, Autism Speaks, Hilibrand Foundation, Genome Canada, OGI, CIHR, and the Simo...

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Detalhes bibliográficos
Autor principal: Marques, Ana Rita (author)
Outros Autores: Martiniano, H. (author), Santos, J.X. (author), Vilela, J. (author), Asif, M. (author), Oliveira, G. (author), Enguita, F.J. (author), Romão, L. (author), Vicente, A.M. (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2018
Assuntos:
Autism Spectrum Disorder
Perturbações do Desenvolvimento Infantil e Saúde Mental
miRNA Gene
lncRNA Gene
Texto completo:http://hdl.handle.net/10400.18/5623
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/5623
Descrição
Resumo:A.R.Marques is recipiente of a fellowship from BioSys PhD programme (Ref PD/BD/113773/2015 from FCT (Portugal). Patients and parents were genotyped in the context of the Autism Genome Project (AGP), funded by NIMH, HRB, MRC, Autism Speaks, Hilibrand Foundation, Genome Canada, OGI, CIHR, and the Simons Simplex Collection (SSC), a core project of the Simons Foundation Autism Research Initiative (SFARI).

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