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Article

Survey of the enthesopathy of X-linked hypophosphatemia and its characterization in Hyp mice.

Calcified tissue international - 1 Sept 2009

Liang Guoying, Katz Lee D, Insogna Karl L, Carpenter Thomas O, Macica Carolyn M

Abstract excerpt

X-linked hypophosphatemia (XLH) is characterized by rickets and osteomalacia as a result of an inactivating mutation of the PHEX (phosphate-regulating gene with homology to endopeptidases on the X chromosome) gene. PHEX encodes an endopeptidase that, when inactivated, results in elevated circulat...

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Source

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Identifiers

PMID: 19609735
DOI: 10.1007/s00223-009-9270-6
PMCID: PMC2988401

Genes

PHEX
FGFR3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19609735-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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