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Clinical and Genetic Characteristics of 153 Chinese Patients With X-Linked Hypophosphatemia
X-linked hypophosphatemia (XLH) is caused by inactivating mutations in the phosphate-regulating endopeptidase homolog, X-linked (PHEX) gene, resulting in an excess of circulating intact fibroblast growth factor-23 (iFGF-23) and a waste of renal phosphate. In the present study, we retrospectively rev...
Tallennettuna:
| Julkaisussa: | Front Cell Dev Biol |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8204109/ https://ncbi.nlm.nih.gov/pubmed/34141703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2021.617738 |
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