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Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life

dc.contributor.authorHerrero Morín, José David 
dc.contributor.authorRodríguez Suárez, Julián 
dc.contributor.authorCoto García, Eliecer 
dc.contributor.authorGil Peña, Helena 
dc.contributor.authorÁlvarez Martínez, María Victoria 
dc.contributor.authorEspinosa Román, Laura
dc.contributor.authorLoris Pablo, César
dc.contributor.authorGil Calvo, Marta
dc.contributor.authorSantos Rodríguez, Fernando 
dc.date.accessioned2013-01-30T10:17:14Z
dc.date.available2013-01-30T10:17:14Z
dc.date.issued2011
dc.identifier.citationNephrology Dialysis Transplantation, 26(1), p. 151-155 (2011); doi:10.1093/ndt/gfq352spa
dc.identifier.issn0931-0509
dc.identifier.urihttp://hdl.handle.net/10651/10126
dc.description.sponsorshipPart of this work was presented at the 4th Joint Meeting of the Spanish and Portuguese Societies of Paediatric Nephrology (Tarragona, Spain, 2005) and at the 32nd Annual Meeting of the Spanish Society of Pediatric Nephrology (Oviedo, Spain, 2006).
dc.format.extentp. 151-155spa
dc.language.isoeng
dc.relation.ispartofNephrology Dialysis Transplantationspa
dc.rights© The Author 2010.
dc.titleGitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of lifespa
dc.typejournal article
dc.identifier.local20110045spa
dc.identifier.doi10.1093/ndt/gfq352
dc.relation.publisherversionhttp://dx.doi.org/10.1093/ndt/gfq352spa


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