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Article

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

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Aug 1997

Meisler M

Abstract excerpt

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Share to Deafness
Share to Endopeptidases
Share to Genes, Dominant
Share to Hypophosphatemia, Familial

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to PHEX Phosphate Regulating Neutral Endopeptidase

Share to Proteins

Share to X Chromosome

Source

Identifiers

PMID: 9250856
DOI: 10.1007/s003359900499

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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A novo missense variant of the PHEX gene in patients with X-linked dominant hypophosphatemiaSemantic proximity Read ↗

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