Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.
- DOI
- 10.1186/s13023-021-01786-5
- Published
- 2021 Apr 1
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-021-01786-5,
title = {Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.},
author = {Rodríguez-Rubio E and Gil-Peña H and Chocron S and Madariaga L and de la Cerda-Ojeda F and Fernández-Fernández M and de Lucas-Collantes C and Gil M and Luis-Yanes MI and Vergara I and González-Rodríguez JD and Ferrando S and Antón-Gamero M and Hidalgo-Barquero MC and Fernández-Escribano A and Fernández-Maseda MÁ and Espinosa L and Oliet A and Vicente A and Ariceta G and Santos F and RenalTubeGroup},
year = {2021},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-021-01786-5},
url = {https://doi.org/10.1186/s13023-021-01786-5}
}RIS
TY - JOUR TI - Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population. AU - Rodríguez-Rubio E AU - Gil-Peña H AU - Chocron S AU - Madariaga L AU - de la Cerda-Ojeda F AU - Fernández-Fernández M AU - de Lucas-Collantes C AU - Gil M AU - Luis-Yanes MI AU - Vergara I AU - González-Rodríguez JD AU - Ferrando S AU - Antón-Gamero M AU - Hidalgo-Barquero MC AU - Fernández-Escribano A AU - Fernández-Maseda MÁ AU - Espinosa L AU - Oliet A AU - Vicente A AU - Ariceta G AU - Santos F AU - RenalTubeGroup PY - 2021 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-021-01786-5 UR - https://doi.org/10.1186/s13023-021-01786-5 ER -
APA
E, R., H, G., S, C., L, M., F, D. L. C., M, F., C, D. L., M, G., MI, L., I, V., JD, G., S, F., M, A., MC, H., A, F., MÁ, F., L, E., A, O., A, V., G, A., F, S., & RenalTubeGroup (2021). Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-021-01786-5
Source records
- pubmed · retrieved 2026-09-27T16:07:27.064Z