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

dc.contributor.author	Gil Calvo, Marta
dc.date.accessioned	2017-06-07T07:10:35Z
dc.date.available	2017-06-07T07:10:35Z
dc.date.issued	2013
dc.identifier.issn	1932-6203
dc.identifier.uri	http://hdl.handle.net/20.500.11940/3468
dc.language.iso	eng
dc.title	Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
dc.type	Artigo	es
dc.authorsophos	Claverie-Martín, F.
dc.authorsophos	García-Nieto, V.
dc.authorsophos	Loris, C.
dc.authorsophos	Ariceta, G.
dc.authorsophos	Nadal, I.
dc.authorsophos	Espinosa, L.
dc.authorsophos	Fernández-Maseda, Á
dc.authorsophos	Antón-Gamero, M.
dc.authorsophos	Avila, Á
dc.authorsophos	Madrid, Á
dc.authorsophos	González-Acosta, H.
dc.authorsophos	Córdoba-Lanus, E.
dc.authorsophos	Santos, F.
dc.authorsophos	Gil-Calvo, M.
dc.authorsophos	Espino, M.
dc.authorsophos	García-Martinez, E.
dc.authorsophos	Sanchez, A.
dc.authorsophos	Muley, R.
dc.identifier.doi	10.1371/journal.pone.0053151
dc.identifier.isi	313480000034
dc.identifier.pmid	23301036
dc.identifier.sophos	13198
dc.issue.number	1
dc.journal.title	PLoS One
dc.organization	Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago - Complexo Hospitalario Universitario de Santiago::Pediatría
dc.rights.accessRights	openAccess
dc.typesophos	Artículo Original
dc.volume.number	8

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