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Article

Early and selective disappearance of telethonin protein from the sarcomere in neurogenic atrophy.

Journal of muscle research and cell motility - 1 Jan 2001

Schröder R, Reimann J, Iakovenko A, Mues A, Bönnemann C G, Matten J, Gautel M

Abstract excerpt

Mutations of the human telethonin gene have recently been shown to cause limb girdle muscular dystrophy type 2G in three Brazilian families. The mRNA has been shown to be dynamically regulated in animals, however, the fate of the protein in human muscle is unknown. In order to assess the expression of telethonin in more frequently encountered myopathological conditions we generated and characterized a rabbit...

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Source

Identifiers

PMID: 11763198
DOI: 10.1023/a:1012242011109

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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