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dc.contributor.authorCouce Pico, María Luz 
dc.contributor.authorBaña Souto, Ana Maria 
dc.date.accessioned2017-06-07T07:17:21Z
dc.date.available2017-06-07T07:17:21Z
dc.date.issued2012
dc.identifier.issn0031-4005
dc.identifier.urihttp://hdl.handle.net/20.500.11940/4743
dc.language.isoeng
dc.titleClinical, genetic, and therapeutic diversity in 2 patients with severe mevalonate kinase deficiency
dc.typeArtigoes
dc.authorsophosGomez, A R
dc.authorsophosCouce, M L
dc.authorsophosGarcia-Villoria, J
dc.authorsophosTorres, A
dc.authorsophosSouto, A B
dc.authorsophosYague, J
dc.authorsophosVilaseca, M A
dc.authorsophosRibes, A
dc.authorsophosArostegui, J I
dc.identifier.doi10.1542/peds.2010-2192
dc.identifier.isi300395100037
dc.identifier.pmid22271696
dc.identifier.sophos7883
dc.issue.number2
dc.journal.titlePEDIATRICS
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Pediatría
dc.page.initiale535
dc.page.finalE539
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number129


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