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Clinical and genetic characteristics of 29 Chinese patients with X-linked hypophosphatemia
OBJECTIVE: The aim of this study was to fully describe the clinical and genetic characteristics, including clinical manifestations, intact fibroblast growth factor 23 (iFGF23) levels, and presence of PHEX gene mutations, of 22 and 7 patients with familial and sporadic X-linked dominant hypophosphate...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437435/ https://www.ncbi.nlm.nih.gov/pubmed/36060934 http://dx.doi.org/10.3389/fendo.2022.956646 |