Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: A case report

dc.contributor.author	Mejía Gaviria, Natalia
dc.contributor.author	Gil Peña, Helena
dc.contributor.author	Coto García, Eliecer
dc.contributor.author	Pérez Menéndez, Teresa M.
dc.contributor.author	Santos Rodríguez, Fernando
dc.date.accessioned	2013-01-30T10:07:41Z
dc.date.available	2013-01-30T10:07:41Z
dc.date.issued	2010
dc.identifier.citation	Orphanet Journal of Rare Diseases, 5(1), (2010); doi:10.1186/1750-1172-5-1PubMed ID: 20074341	spa
dc.identifier.issn	1750-1172
dc.identifier.uri	http://hdl.handle.net/10651/8372
dc.language.iso	eng
dc.relation.ispartof	Orphanet Journal of Rare Diseases	spa
dc.rights	(c) Orphanet Journal of Rare Diseases
dc.source	Scopus	spa
dc.source.uri	http://www.scopus.com/inward/record.url?eid=2-s2.0-77049107749&partnerID=40&md5=2b91e4a2fd32ae53c74f154cb915b021
dc.title	Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: A case report	spa
dc.type	journal article
dc.identifier.local	20100196	spa
dc.identifier.doi	10.1186/1750-1172-5-1PubMed ID: 20074341
dc.relation.publisherversion	http://dx.doi.org/10.1186/1750-1172-5-1	spa
dc.rights.accessRights	open access