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dc.contributor.authorFachal Vilar, Laura
dc.contributor.authorToribio Pérez, Jaime 
dc.contributor.authorVega Gliemmo, Ana
dc.contributor.authorGinarte Val, Manuel Javier
dc.contributor.authorCarracedo Álvarez, Ángel
dc.contributor.authorRodríguez Pazos, Laura 
dc.date.accessioned2017-06-07T07:10:29Z
dc.date.available2017-06-07T07:10:29Z
dc.date.issued2011
dc.identifier.issn0007-0963
dc.identifier.urihttp://hdl.handle.net/20.500.11940/3447
dc.language.isoeng
dc.titleAnalysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.
dc.typeArtigoes
dc.authorsophosRodriguez-Pazos, L.
dc.authorsophosGinarte, M.
dc.authorsophosFachal, L.
dc.authorsophosToribio, J.
dc.authorsophosCarracedo, A.
dc.authorsophosVega, A.;
dc.identifier.doi10.1111/j.1365-2133.2011.10454.x
dc.identifier.isi295285500027
dc.identifier.pmid21668430
dc.identifier.sophos9828
dc.issue.number4
dc.journal.titleBRITISH JOURNAL OF DERMATOLOGY
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Dermatoloxía
dc.page.initial906
dc.page.final911
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number165


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