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...

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Detalles Bibliográficos
Autores principales: Xu, Tian, Tao, Xiaohui, Zhang, Zhenlin, Yue, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Endocrinology
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

Internet

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

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