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Article

Asymmetric phenotype associated with rare myelin protein zero mutation.

Journal of clinical neuromuscular disease - 1 Mar 2010

Souayah Nizar, Tick Chong Peter Siao

Abstract excerpt

Myelin protein zero (MPZ) mutations cause demyelinating neuropathies that range from severe neonatal to milder adult forms. We report a 36-year-old man who developed weakness of his left little finger adduction 3 years earlier. The weakness progressed to his other limbs. Examination revealed mild...

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Source

Identifiers

PMID: 20215982
DOI: 10.1097/CND.0b013e3181c5058a

Genes

MPZ

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20215982-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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