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dc.contributor.authorFernández Marmiesse, Ana 
dc.date.accessioned2017-06-07T07:06:34Z
dc.date.available2017-06-07T07:06:34Z
dc.date.issued2015
dc.identifier.issn1664-8021
dc.identifier.urihttp://hdl.handle.net/20.500.11940/2700
dc.language.isoeng
dc.titleCorrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations
dc.typeArtigoes
dc.authorsophosBrito, S.
dc.authorsophosThompson, K.
dc.authorsophosCampistol, J.
dc.authorsophosColomer, J.
dc.authorsophosHardy, S. A.
dc.authorsophosHe, L.
dc.authorsophosFernandez-Marmiesse, A.
dc.authorsophosPalacios, L.
dc.authorsophosJou, C.
dc.authorsophosJimenez-Mallebrera, C.
dc.authorsophosArmstrong, J.
dc.authorsophosMontero, R.
dc.authorsophosArtuch, R.
dc.authorsophosTischner, C.
dc.authorsophosWenz, T.
dc.authorsophosMcFarland, R.
dc.authorsophosTaylor, R. W.
dc.identifier.doi10.3389/fgene.2015.00254
dc.identifier.pmid26284110
dc.identifier.sophos18579
dc.issue.number5
dc.journal.titleFrontiers in Genetics
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Hematoloxía clínica
dc.page.initial254
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number6


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