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Copy number variants involving components of the glutamatergic synaptic pathway in ASD patients

dc.contributor.authorOliveira, B.A.
dc.contributor.authorConceição, I.C.
dc.contributor.authorCorreia, C.A.
dc.contributor.authorCafé, C.
dc.contributor.authorAlmeida, J.
dc.contributor.authorMouga, S.
dc.contributor.authorDuque, F.
dc.contributor.authorOliveira, G.
dc.contributor.authorVicente, A.M.
dc.date.accessioned2012-11-27T11:06:01Z
dc.date.available2012-11-27T11:06:01Z
dc.date.issued2012-11
dc.descriptionThis work was supported by the fellowships SFRH/BD/79081/2011 to BO, SFRH/BPD/74739/2010 to ICC and SFRH/BPD/64281/2009 to CC from Fundação para a Ciência e a Tecnologia (FCT; Portugal).por
dc.description.abstractCopy Number Variants (CNVs) play an important role in susceptibility to Autism Spectrum Disorders (ASD), in particular when deleting or duplicating genes involved in synaptic structure and function such as glutamatergic synapse genes. Identifying CNVs of etiologic relevance for ASD that include glutamatergic genes may contribute to the understanding of glutamate-related pathogenic mechanisms in this disorder.por
dc.identifier.urihttp://hdl.handle.net/10400.18/1120
dc.language.isoengpor
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpor
dc.subjectPerturbações do Desenvolvimento Infantil e Saúde Mentalpor
dc.subjectAutismpor
dc.subjectASDpor
dc.titleCopy number variants involving components of the glutamatergic synaptic pathway in ASD patientspor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlacePorto, Portugalpor
oaire.citation.title16ª Reunião Anual da Sociedade Portuguesa de Genética Humana, 22-24 Novembro 2012por
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor

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