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Article

A mutation in CHN-1/CHIP suppresses muscle degeneration in Caenorhabditis elegans.

Developmental biology - 1 Dec 2007

Nyamsuren Oyunbileg, Faggionato Davide, Loch Wiebke, Schulze Ekkehard, Baumeister Ralf

Abstract excerpt

Duchenne muscular dystrophy (DMD) is one of the most severe X-linked, inherited diseases of childhood, characterized by progressive muscle wasting and weakness as the consequence of mutations in the dystrophin gene. The protein encoded by dystrophin is a huge cytosolic protein that links the intracellular F-actin filaments to the members of the dystrophin-glycoprotein-complex (DGC). Dystrophin deficiency results...

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Source

Identifiers

PMID: 17961535
DOI: 10.1016/j.ydbio.2007.09.033

Genes

DMD

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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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