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Autism Spectrum Disorder: modulation of genomic variant effects on brain structure and function

dc.contributor.authorVilela, Joana
dc.contributor.authorMartiniano, Hugo
dc.contributor.authorMarques, Ana Rita
dc.contributor.authorXavier Santos, João
dc.contributor.authorAsif, Muhammad
dc.contributor.authorRasga, Célia
dc.contributor.authorOliveira, Guiomar
dc.contributor.authorVicente, Astrid M.
dc.date.accessioned2019-02-13T11:02:02Z
dc.date.available2019-02-13T11:02:02Z
dc.date.issued2018-07
dc.descriptionJoana 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.pt_PT
dc.description.abstractThe 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.pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/5776
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.subjectAutism Spectrum Disorderpt_PT
dc.subjectSingle Nucleotide Variantspt_PT
dc.subjectAutismopt_PT
dc.subjectPerturbações do Desenvolvimento Infantil e Saúde Mentalpt_PT
dc.titleAutism Spectrum Disorder: modulation of genomic variant effects on brain structure and functionpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboa, Portugalpt_PT
oaire.citation.titleCiência 2018 - Encontro com a Ciência e Tecnologia em Portugal, 2-4 julho 2018pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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