A case report of autosomal dominant hypophosphatemic rickets due to a mutation in the  FGF23  gene in an adult: diagnostic difficulties

E. E. Sakhnova; E. G. Przhiyalkovskaya; E. O. Mamedova; I. S. Chugunov

doi:10.14341/osteo13178-10323

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Sakhnova E.E., Przhiyalkovskaya E.G., Mamedova E.O., Chugunov I.S. A case report of autosomal dominant hypophosphatemic rickets due to a mutation in the FGF23 gene in an adult: diagnostic difficulties. Osteoporosis and Bone Diseases. 2024;27(4):17-24. (In Russ.) https://doi.org/10.14341/osteo13178

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This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND 4.0).

ISSN 2072-2680 (Print)
ISSN 2311-0716 (Online)

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Osteoporosis and Bone Diseases

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