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Article

Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype.

Muscle & nerve - 1 Jan 1994

Hoogendijk J E, De Visser M, Bolhuis P A, Hart A A, Ongerboer de Visser B W

Abstract excerpt

Forty-four affected individuals, aged 8-68 years (mean 34 years), from six families with hereditary motor and sensory neuropathy type I (HMSN I, Charcot-Marie-Tooth disease type 1) were investigated to determine the clinical and electroneurographical characteristics of the HMSN I subtype that is defined by the presence of a DNA duplication on chromosome 17p. Motor nerve conduction velocity (MNCV) and, to a lesser...

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Identifiers

PMID: 8264707
DOI: 10.1002/mus.880170112

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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