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Article

The PEX gene: its role in X-linked rickets, osteomalacia, and bone mineral metabolism.

Experimental nephrology - 1 Jan 2000

Rowe P S

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Share to Bone Density
Share to Cloning, Molecular
Share to Hypophosphatemia, Familial
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to PHEX Phosphate Regulating Neutral Endopeptidase

Share to Proteins

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PMID: 9386970

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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The PEX gene: its role in X-linked rickets, osteomalacia, and bone mineral metabolism.PMID 9386970Read ↗

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A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic ricketsSemantic proximity Read ↗

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[X-linked hypophosphatemic rickets due to mutations in PHEX: Clinical and evolutionary variability].Semantic proximity Read ↗

Two novel PHEX mutations in Taiwanese patients with X-linked hypophosphatemic rickets.Semantic proximity Read ↗

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Novel PHEX mutation associated with hypophosphatemic rickets.Semantic proximity Read ↗

[Molecular aspects of familial hypophosphatemic rickets].Semantic proximity Read ↗

Three novel mutations of the PHEX gene in three Chinese families with X-linked dominant hypophosphatemic rickets.Semantic proximity Read ↗

Mutation watch: PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness.Semantic proximity Read ↗

Functional Characterization of PHEX Gene Variants in Children With X-Linked Hypophosphatemic Rickets Shows No Evidence of Genotype-Phenotype Correlation.Semantic proximity Read ↗

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