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dc.contributor.authorArrojo Romero, Manuel 
dc.contributor.authorPaz Silva, Eduardo 
dc.contributor.authorBrenlla González, Julio
dc.contributor.authorCostas Costas, Javier 
dc.contributor.authorPáramo Fernández, Mario 
dc.contributor.authorGonzález Penas, Javier
dc.date.accessioned2017-06-07T07:35:07Z
dc.date.available2017-06-07T07:35:07Z
dc.date.issued2015
dc.identifier.issn1552-4841
dc.identifier.urihttp://hdl.handle.net/20.500.11940/8229
dc.language.isoeng
dc.titleCumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility
dc.typeArtigoes
dc.authorsophosGonzález-Peñas, J.
dc.authorsophosArrojo, M.
dc.authorsophosPaz, E.
dc.authorsophosBrenlla, J.
dc.authorsophosPáramo, M.
dc.authorsophosCostas, J.
dc.identifier.doi10.1002/ajmg.b.32324
dc.identifier.isi361221200002
dc.identifier.pmid25982957
dc.identifier.sophos19574
dc.issue.number7
dc.journal.titleAMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Psiquiatría
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago::IDIS.- Instituto de investigaciones sanitarias de Santiago
dc.page.initial528
dc.page.final535
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number168


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