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Article

FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate.

Biochemical and biophysical research communications - 22 Jun 2001

Bowe A E, Finnegan R, Jan de Beur S M, Cho J, Levine M A, Kumar R, Schiavi S C

Abstract excerpt

Oncogenic osteomalacia (OOM), X-linked hypophosphatemia (XLH), and autosomal dominant hypophosphatemic rickets (ADHR) are phenotypically similar disorders characterized by hypophosphatemia, decreased renal phosphate reabsorption, normal or low serum calcitriol concentrations, normal serum concentrations of calcium and parathyroid hormone, and defective skeletal mineralization. XLH results from mutations in the...

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Source

Identifiers

PMID: 11409890
DOI: 10.1006/bbrc.2001.5084

Genes

PHEX

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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