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Article

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.

Ophthalmology - 1 May 1994

Sigesmund D A, Weleber R G, Pillers D A, Westall C A, Panton C M, Powell B R, Héon E, Murphey W H, Musarella M A, Ray P N

Abstract excerpt

PURPOSE: Dystrophin, the Duchenne muscular dystrophy gene product, has been localized to the outer plexiform layer of normal human retina. The purpose of this study is to define completely the ocular phenotype associated with mutations at Xp21, the Duchenne muscular dystrophy gene locus. METHODS: Twenty-one patients with a diagnosis of Duchenne muscular dystrophy and five patients with Becker muscular dystrophy...

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Source

Identifiers

PMID: 8190471
DOI: 10.1016/s0161-6420(13)31249-4

Genes

ERG

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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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Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.PMID 8190471Read ↗

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