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Article

Abnormal junctions and permeability of myelin in PMP22-deficient nerves.

Annals of neurology - 1 Feb 2014

Guo Jiasong, Wang Leiming, Zhang Yang, Wu Jiawen, Arpag Sezgi, Hu Bo, Imhof Beat A, Tian Xinxia, Carter Bruce D, Suter Ueli, Li Jun

Abstract excerpt

OBJECTIVE: The peripheral myelin protein-22 (PMP22) gene is associated with the most common types of inherited neuropathies, including hereditary neuropathy with liability to pressure palsies (HNPP) caused by PMP22 deficiency. However, the function of PMP22 has yet to be defined. Our previous stu...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 24339129
DOI: 10.1002/ana.24086
PMCID: PMC4206215

Genes

PMP22
MAG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24339129-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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