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Article

[Mutation of the myelin Po gene in hereditary motor and sensory neuropathy].

Rinsho shinkeigaku = Clinical neurology - 1 Dec 1995

Hayasaka K

Abstract excerpt

Charcot-Marie-Tooth neuropathy type 1 (CMT1) or hereditary motor and sensory neuropathy (HMSN1) is the most common inherited peripheral neuropathy. Most cases show dominant inheritance. CMT1 loci map to chromosome 17 (CMT1A), chromosome 1 (CMT1B), another unknown autosome (CMT1C) and the X chromo...

Topics

Charcot-Marie-Tooth Disease
Chromosomes, Human, Pair 1
Hereditary Sensory and Motor Neuropathy
Humans
Mutation
Myelin P0 Protein

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8752425

Genes

PMP22

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8752425-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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