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Navegación por Autor Vilches, Susana
Mostrando resultados 1 a 3 de 3
Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
openAccess | | 28-may-2022 | A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2 | Errasti, Suriel; Peñalva, Mercedes; Recio-Poveda, Lucía ; Vilches, Susana; Casado-Vela, Juan CSIC ORCID CVN; Pérez Pérez, Julián; Botella, Luisa María CSIC ORCID ; Albiñana, Virginia CSIC; Cuesta, Ángel M. CSIC ORCID | artículo |
openAccess | | oct-2016 | An 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. | Pérez Pérez, J.; Olavarrieta, Leticia CSIC; Vilches, Susana; Diaz Jauregui, T.; López-Trascasa, Margarita; Sánchez-Corral, Pilar CSIC ORCID; Arjona, Emilia CSIC ORCID ; Rodríguez de Córdoba, Santiago | comunicación de congreso |
closedAccess | | 14-abr-2021 | Detection of genetic rearrangements in the regulators of complement activation RCA cluster by high-throughput sequencing and MLPA | García-Fernández, Jesús CSIC ; Vilches, Susana; Olavarrieta, Leticia CSIC; Pérez Pérez, J.; Rodríguez de Córdoba, Santiago | capítulo de libro |