Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population (Orphanet Journal of Rare Diseases, (2021), 16, 1, (104), 10.1186/s13023-021-01729-0)

Rodríguez-Rubio, Enrique; Gil-Peña, Helena; Chocrón, Sara; Madariaga, Leire; de-la-Cerda-Ojeda, Francisco; Fernández-Fernández, Marta; de-Lucas-Collantes, Carmen; Gil, Marta; Luis-Yanes, María-Isabel; Vergara, Inés; González-Rodríguez, Juan-David; Ferrando, Susana; Antón-Gamero, Montserrat; Carrasco-Hidalgo-Barquero, Marta; Fernández-Escribano, Angustias; Fernández-Maseda, María-Ángeles; Espinosa, Laura; Oliet, Aniana; Vicente, Antonio; Ariceta, G; Santos, Fernando

RICSMUR Principal
→
02. Servicio Murciano de Salud (SMS)
→
02.02. Área de Salud II Cartagena
→
02.02.01. Investigación y comunicación científica
→
Ver ítem

dc.contributor.author	Rodríguez-Rubio, Enrique
dc.contributor.author	Gil-Peña, Helena
dc.contributor.author	Chocrón, Sara
dc.contributor.author	Madariaga, Leire
dc.contributor.author	de-la-Cerda-Ojeda, Francisco
dc.contributor.author	Fernández-Fernández, Marta
dc.contributor.author	de-Lucas-Collantes, Carmen
dc.contributor.author	Gil, Marta
dc.contributor.author	Luis-Yanes, María-Isabel
dc.contributor.author	Vergara, Inés
dc.contributor.author	González-Rodríguez, Juan-David
dc.contributor.author	Ferrando, Susana
dc.contributor.author	Antón-Gamero, Montserrat
dc.contributor.author	Carrasco-Hidalgo-Barquero, Marta
dc.contributor.author	Fernández-Escribano, Angustias
dc.contributor.author	Fernández-Maseda, María-Ángeles
dc.contributor.author	Espinosa, Laura
dc.contributor.author	Oliet, Aniana
dc.contributor.author	Vicente, Antonio
dc.contributor.author	Ariceta, G
dc.contributor.author	Santos, Fernando
dc.date.accessioned	2025-05-06T10:42:03Z
dc.date.available	2025-05-06T10:42:03Z
dc.date.issued	2021
dc.identifier.citation	Rodríguez-Rubio E, Gil-Peña H, Chocron S, Madariaga L, de la Cerda-Ojeda F, Fernández-Fernández M, et al. Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population. Orphanet J Rare Dis. 1 de abril de 2021;16(1):154.
dc.identifier.uri	https://sms.carm.es/ricsmur/handle/123456789/18843
dc.language.iso	eng
dc.publisher	BioMed Central Ltd
dc.rights	Atribución-NoComercial-SinDerivadas 4.0 España
dc.rights.uri	https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es	*
dc.title	Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population (Orphanet Journal of Rare Diseases, (2021), 16, 1, (104), 10.1186/s13023-021-01729-0)
dc.type	info:eu-repo/semantics/article
dc.identifier.pmid	33794951
dc.relation.publisherversion	https://dx.doi.org/10.1186/s13023-021-01786-5
dc.type.version	info:eu-repo/semantics/publishedVersion
dc.identifier.doi	10.1186/s13023-021-01786-5
dc.journal.title	Orphanet Journal of Rare Diseases
dc.identifier.essn	1750-1172