A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma

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dc.contributor.authorMéndez, Manuelspa
dc.contributor.authorPoblete-Gutiérrez, Pamelaspa
dc.contributor.authorMorán-Jiménez, María Josefaspa
dc.contributor.authorRodriguez, M. E.spa
dc.contributor.authorGarrido Astray, María Concepción
dc.contributor.authorFontanellas, Antoniospa
dc.contributor.authorFrank, Jorgespa
dc.contributor.authorEnríquez de Salamanca, Rafaelspa
dc.date.accessioned2013-11-27T17:26:32Z
dc.date.available2013-11-27T17:26:32Z
dc.date.issued2009spa
dc.description.impact2.547 JCR (2009) Q1, 8/73 Sport sciencesspa
dc.identifier.citationMéndez, M., Poblete‐Gutiérrez, P., Morán‐Jiménez, M. J., Rodríguez, M. E., Garrido‐Astray, M. C., Fontanellas, A., ..., & Enríquez-Salamanca, R. (2009). A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma. British Journal of Dermatology, 160(6), 1330-1334.spa
dc.identifier.doi10.1111/j.1365-2133.2009.09084.xspa
dc.identifier.urihttp://hdl.handle.net/11268/820
dc.language.isoengspa
dc.peerreviewedSispa
dc.rights.accessRightsrestricted accessen
dc.subject.unescoEnfermedades de la pielspa
dc.titleA homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratodermaspa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublication7672ac67-5a02-40ad-a3b2-94c3449b9966
relation.isAuthorOfPublication.latestForDiscovery7672ac67-5a02-40ad-a3b2-94c3449b9966

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