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Article

Steroid responsive polyneuropathy in a family with a novel myelin protein zero mutation.

Journal of neurology, neurosurgery, and psychiatry - 1 Dec 2000

Donaghy M, Sisodiya S M, Kennett R, McDonald B, Haites N, Bell C

Abstract excerpt

OBJECTIVE: To report a novel hereditary motor and sensory neuropathy (HMSN) phenotype, with partial steroid responsiveness, caused by a novel dominant mutation in the myelin protein zero (MPZ) gene. Most MPZ mutations lead to the HMSN type I phenotype, with recent reports of Déjérine-Sottas, cong...

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Source

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Identifiers

PMID: 11080236
DOI: 10.1136/jnnp.69.6.799
PMCID: PMC1737181

Genes

MPZ

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-11080236-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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