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Oral Iron Replacement Normalizes Fibroblast Growth Factor 23 in Iron Deficient Patients with Autosomal Dominant Hypophosphatemic Rickets

Autosomal dominant hypophosphatemic rickets (ADHR) is caused by mutations impairing cleavage of fibroblast growth factor 23 (FGF23). FGF23 gene expression increases during iron deficiency. In humans and mice with the ADHR mutation, iron deficiency results in increased intact FGF23 concentrations and...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:J Bone Miner Res
मुख्य लेखकों: Imel, Erik A., Liu, Ziyue, Coffman, Melissa, Acton, Dena, Mehta, Rakesh, Econs, Michael J.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 2019
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC7333537/
https://ncbi.nlm.nih.gov/pubmed/31652009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.3878
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