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Article

[Oculopharyngeal muscular dystrophy. A census of French families and genealogic study].

Revue neurologique - 1 Jan 1990

Brunet G, Tomé F M, Samson F, Robert J M, Fardeau M

Abstract excerpt

The first results of a collaborative study aimed at collecting all French families affected by oculopharyngeal muscular dystrophy (OPMD) and their genealogy are presented. The study was carried out in 28 families in whom the diagnosis of OPMD in the propositus was confirmed by the presence of typical intranuclear tubulo-filamentous inclusions in the muscle biopsy. Results suggest that the prevalence of OPMD in...

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Source

Identifiers

PMID: 2204987

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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