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Article

Human nerve pathology caused by different mutational mechanisms of the PMP22 gene.

Annals of the New York Academy of Sciences - 14 Sept 1999

Gabreëls-Festen A, Wetering R V

Abstract excerpt

The study of the morphological phenotypes in patients with different mutations of the PMP22 gene gives additional insights into the role of the protein in myelin function. The pathology in young patients is in some aspects different from the pathology in older patients, providing essential and additional information about the early disease processes in humans induced by different PMP22 mutational mechanisms....

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Source

Identifiers

PMID: 10586258

Genes

PMP22

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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