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Article

Natural history and treatment of peripheral inherited neuropathies.

Advances in experimental medicine and biology - 1 Jan 2009

Pareyson Davide, Marchesi Chiara

Abstract excerpt

Charcot-Marie-Tooth disease (CMT) is genetically highly heterogeneous. Disease course and severity vary according to CMT type, causative gene, and mutation type, but considerable phenotypic variability may occur also for the same CMT type. Research is focused on possible modifier factors particularly in CMT1A associated with Peripheral Myelin Protein 22 (PMP22) overexpression. Natural history studies are...

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Identifiers

PMID: 20225028
DOI: 10.1007/978-90-481-2813-6_14

Genes

PMP22

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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