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Article

Charcot-Marie-Tooth syndrome.

Archives of neurology - 1 Nov 1993

Chance P F, Pleasure D

Abstract excerpt

Charcot-Marie-Tooth syndrome (CMT) is a group of genetically determined symmetric distal polyneuropathies. The CMT loci are known to map to chromosome 1 (CMT1B), chromosome 17 (CMT1A), the X chromosome (CMTX), and two additional unknown autosomes (CMT1C and CMT2). The most prevalent form is CMT1A...

Topics

Animals
Charcot-Marie-Tooth Disease
Chromosome Banding
Chromosome Mapping
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 17
Crossing Over, Genetic
Gene Deletion
Genetic Linkage
Humans
Meiosis
Mice
Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Myelin Proteins

Peripheral Nervous System Diseases

Repetitive Sequences, Nucleic Acid

X Chromosome

Source

Identifiers

PMID: 8215977
DOI: 10.1001/archneur.1993.00540110060006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8215977-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

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

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