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dc.contributor.authorPérez Pérez, J.es_ES
dc.contributor.authorOlavarrieta, Leticiaes_ES
dc.contributor.authorVilches, S.es_ES
dc.contributor.authorDiaz Jauregui, T.es_ES
dc.contributor.authorLópez-Trascasa, Margaritaes_ES
dc.contributor.authorSánchez-Corral, Pilares_ES
dc.contributor.authorArjona, Emiliaes_ES
dc.contributor.authorRodríguez de Córdoba, Santiagoes_ES
dc.date.accessioned2016-10-11T12:38:50Z-
dc.date.available2016-10-11T12:38:50Z-
dc.date.issued2016-10-
dc.identifier.citationPediatr Nephrol 31 (10): 1871 (2016)es_ES
dc.identifier.issn0931-041X-
dc.identifier.urihttp://hdl.handle.net/10261/137985-
dc.description1 p. Abstracts for the 17th IPNA Congress, Iguaçu, Brazil, September 2016es_ES
dc.language.isoenges_ES
dc.publisherSpringeres_ES
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccessen_EN
dc.titleAn retrospective analysis of genetic diagnosis in Atypical Hemolytic Uremic Syndrome (aHUS) and C3 glomerulopathy (C3G). Where we are now and where we are moving to.es_ES
dc.typecomunicación de congresoes_ES
dc.identifier.doi10.1007/s00467-016-3467-5-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/ 10.1007/s00467-016-3467-5es_ES
dc.identifier.e-issn1432-198X-
dc.embargo.terms2017-11-01es_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
Appears in Collections:(CIB) Comunicaciones congresos
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