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Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

dc.contributor.authorGil Calvo, Marta 
dc.date.accessioned2017-06-07T07:10:35Z
dc.date.available2017-06-07T07:10:35Z
dc.date.issued2013
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/20.500.11940/3468
dc.language.isoeng
dc.titleClaudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
dc.typeArtigoes
dc.authorsophosClaverie-Martín, F.
dc.authorsophosGarcía-Nieto, V.
dc.authorsophosLoris, C.
dc.authorsophosAriceta, G.
dc.authorsophosNadal, I.
dc.authorsophosEspinosa, L.
dc.authorsophosFernández-Maseda, Á
dc.authorsophosAntón-Gamero, M.
dc.authorsophosAvila, Á
dc.authorsophosMadrid, Á
dc.authorsophosGonzález-Acosta, H.
dc.authorsophosCórdoba-Lanus, E.
dc.authorsophosSantos, F.
dc.authorsophosGil-Calvo, M.
dc.authorsophosEspino, M.
dc.authorsophosGarcía-Martinez, E.
dc.authorsophosSanchez, A.
dc.authorsophosMuley, R.
dc.identifier.doi10.1371/journal.pone.0053151
dc.identifier.isi313480000034
dc.identifier.pmid23301036
dc.identifier.sophos13198
dc.issue.number1
dc.journal.titlePLoS One
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Pediatría
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number8


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