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Article

Connexin 32 mutation in a Turkish family with X-linked Charcot-Marie-Tooth disease.

The International journal of neuroscience - 1 Jun 2003

Sahin Nilufer, Tan Meliha, Kalay Ersan, Calapoglu Mustafa, Karaguzel Ahmet

Abstract excerpt

In the present work, we describe a large Turkish family (N=39) with Charcot-Marie-Tooth disease, which is the most commonly inherited peripheral neuropathy. The subjects were from four generations, including six hemizygote patients and nine heterozygote carrier females. Symptoms appeared in late...

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Source

Identifiers

PMID: 12775342
DOI: 10.1080/00207450390200972

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12775342-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

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

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