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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)

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dc.contributor.author Rodríguez-Rubio, Enrique
dc.contributor.author Gil-Peña, Helena
dc.contributor.author Chocron, 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 Hidalgo-Barquero, Marta-Carrasco
dc.contributor.author Fernández-Escribano, Angustias
dc.contributor.author Fernández-Maseda, Mº-Ángeles
dc.contributor.author Espinosa, Laura
dc.contributor.author Oliet, Aniana
dc.contributor.author Vicente, Antonio
dc.contributor.author Ariceta, Gema
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.issn 1750-1172
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


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Atribución-NoComercial-SinDerivadas 4.0 España Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución-NoComercial-SinDerivadas 4.0 España

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