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Gitelman syndrome: a review of clinical features, genetic diagnosis and therapeutic management

dc.contributor.authorSantos Rodríguez, Fernando 
dc.contributor.authorGil Peña, Helena 
dc.contributor.authorBlázquez, Cristina
dc.contributor.authorCoto García, Eliecer 
dc.date.accessioned2017-02-22T10:34:45Z
dc.date.available2017-02-22T10:34:45Z
dc.date.issued2016
dc.identifier.citationExpert Opinion on Orphan Drugs, 4(10), p. 1005-1009 (2016); doi:10.1080/21678707.2016.1223542
dc.identifier.issn2167-8707
dc.identifier.urihttp://hdl.handle.net/10651/40520
dc.description.sponsorshipThis paper was funded by Ministerio de Economía y Competitividad, Instituto de Salud Carlos III (PI14/00702) and Fondos Feder.
dc.format.extentp. 1005-1009
dc.language.isoeng
dc.relation.ispartofExpert Opinion on Orphan Drugs
dc.rights©,
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84988956426&partnerID=40&md5=b646bd4eb772d758a67db921a84c109b
dc.titleGitelman syndrome: a review of clinical features, genetic diagnosis and therapeutic management
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1080/21678707.2016.1223542
dc.type.dcmitext
dc.relation.projectIDMinisterio de Economía y Competitividad, Instituto de Salud Carlos III (PI14/00702)
dc.relation.publisherversionhttp://dx.doi.org/10.1080/21678707.2016.1223542


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