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Article

Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina.

Human molecular genetics - 1 Jul 2003

Dalloz Cécile, Sarig Rachel, Fort Patrice, Yaffe David, Bordais Agnès, Pannicke Thomas, Grosche Jens, Mornet Dominique, Reichenbach Andreas, Sahel José, Nudel Uri, Rendon Alvaro

Abstract excerpt

The abnormal retinal neurotransmission observed in Duchenne muscular dystrophy (DMD) patients and in some genotypes of mice lacking dystrophin has been attributed to altered expression of short products of the dystrophin gene. We have investigated the potential role of Dp71, the most abundant C-t...

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Source

Identifiers

PMID: 12812982
DOI: 10.1093/hmg/ddg170

Genes

AQP4
DMD
ERG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12812982-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina.PMID 12812982Read ↗

Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retina.Semantic proximity Read ↗

The Multi-System Roles of Dp71 Dystrophin Isoforms in Duchenne Muscular DystrophySemantic proximity Read ↗

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Dystrophin-gene mutation location influences severity of electroretinogram defects in mouse models of Duchenne muscular dystrophy.Semantic proximity Read ↗

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