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Article

Molecular genetics of X-linked Charcot-Marie-Tooth disease.

Neuromolecular medicine - 1 Jan 2006

Kleopa Kleopas A, Scherer Steven S

Abstract excerpt

The X-linked form of Charcot-Marie-Tooth disease (CMT1X) is the second most common molecularly designated form of hereditary motor and sensory neuropathy. The clinical phenotype is characterized by progressive distal muscle atrophy and weakness, areflexia, and variable sensory abnormalities. Affe...

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Source

Identifiers

PMID: 16775370
DOI: 10.1385/nmm:8:1-2:107

Genes

GJB1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16775370-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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