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Article

Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.

Brain : a journal of neurology - 1 Jul 2000

Krajewski K M, Lewis R A, Fuerst D R, Turansky C, Hinderer S R, Garbern J, Kamholz J, Shy M E

Abstract excerpt

Charcot-Marie-Tooth disease type 1A (CMT1A), the most frequent form of CMT, is caused by a 1.5 Mb duplication on the short arm of chromosome 17. Patients with CMT1A typically have slowed nerve conduction velocities (NCVs), reduced compound motor and sensory nerve action potentials (CMAPs and SNAP...

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Source

Identifiers

PMID: 10869062
DOI: 10.1093/brain/123.7.1516

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-10869062-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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