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Article

Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.

Journal of neurology - 1 Jan 2004

Arning Larissa, Jagiello Peter, Schara Ulrike, Vorgerd Matthias, Dahmen Norbert, Gencikova Alexandra, Mortier Wilhelm, Epplen Jörg T, Gencik Martin

Abstract excerpt

Mutations in genes coding for the dystrophin-glycoprotein complex (DGC) cause inherited muscular dystrophies (MD), including Morbus Duchenne (DMD) and M. Becker (BMB) as well as limb-girdle muscular dystrophies (LGMD). New insights into the pathophysiology of the dystrophic muscle, the identification of compensatory mechanisms and additional proteins interacting with dystrophin are essential for developing new...

Read the complete abstract on PubMed

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Muscles

Share to Muscular Dystrophies

Share to Muscular Dystrophy, Duchenne

Share to Reverse Transcriptase Polymerase Chain Reaction

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Source

Identifiers

PMID: 14999492
DOI: 10.1007/s00415-004-0274-x

Genes

DMD

Provenance

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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Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.PMID 14999492Read ↗

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