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Article

Oculopharyngeal muscle dystrophy: fine structure and mRNA expression levels of PABPN1.

Clinical neuropathology - 1 Jan 2000

Schröder J M, Klossok T, Weis J

Abstract excerpt

OBJECTIVE: The underlying molecular mechanism leading to the OPMD causing mutation in the PABPN1 gene has not been elucidated so far. Two models are under consideration: the first model is the polymerase slippage mechanism. The second model is unequal crossing over. The aim of the present study i...

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Topics

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Share to Gene Expression Regulation
Share to Intranuclear Inclusion Bodies
Share to Microscopy, Electron, Transmission

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscle, Skeletal

Share to Muscle Weakness

Share to Muscular Dystrophy, Oculopharyngeal

Share to Reverse Transcriptase Polymerase Chain Reaction

Share to Trinucleotide Repeat Expansion

Source

Identifiers

PMID: 21545772
DOI: 10.5414/npp30094

Genes

GCG
PABPN1
GCA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21545772-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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Oculopharyngeal muscle dystrophy: fine structure and mRNA expression levels of PABPN1.PMID 21545772Read ↗

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