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Complex III deficiency in a Portuguese family: expanding the clinical phenotype

dc.contributor.authorNogueira, Célia
dc.contributor.authorNesti, Claudia
dc.contributor.authorMeschini, M. Clara
dc.contributor.authorCarrozzo, Rosalba
dc.contributor.authorBarros, José
dc.contributor.authorSá, Maria José
dc.contributor.authorAzevedo, Luisa
dc.contributor.authorSantorelli, Filippo
dc.contributor.authorVilarinho, Laura
dc.date.accessioned2014-03-18T13:02:13Z
dc.date.available2014-03-18T13:02:13Z
dc.date.issued2013-09
dc.identifier.urihttp://hdl.handle.net/10400.18/2166
dc.language.isoengpor
dc.subjectCIIIpor
dc.subjectDoenças Genéticaspor
dc.titleComplex III deficiency in a Portuguese family: expanding the clinical phenotypepor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceBarcelona, Espanhapor
oaire.citation.title12th International Congress of Inborn Errors of Metabolism (ICIEM), 3-6 September 2013por
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor

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