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Article

Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene.

Journal of neurology, neurosurgery, and psychiatry - 1 Feb 1999

Bähr M, Andres F, Timmerman V, Nelis M E, Van Broeckhoven C, Dichgans J

Abstract excerpt

BACKGROUND: X linked dominant Charcot-Marie-Tooth disease (CMT1X) is an inherited motor and sensory neuropathy that mainly affects the peripheral nervous system. CMT1X is associated with mutations in the gap junction protein connexin 32 (Cx32). Cx32 is expressed in Schwann cells and oligodendrocy...

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Source

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Identifiers

PMID: 10071100
DOI: 10.1136/jnnp.66.2.202
PMCID: PMC1736220

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-10071100-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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