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Article

Electron transfer flavoprotein deficiency: functional and molecular aspects.

Molecular genetics and metabolism - 1 Jun 2006

Schiff Manuel, Froissart Roseline, Olsen Rikke K J, Acquaviva Cécile, Vianey-Saban Christine

Abstract excerpt

Multiple acyl-CoA dehydrogenase deficiency (MADD) is a recessively inherited metabolic disorder that can be due to a deficiency of electron transfer flavoprotein (ETF) or its dehydrogenase (ETF-ubiquinone oxidoreductase). ETF is a mitochondrial matrix protein consisting of alpha- (30kDa) and beta- (28kDa) subunits encoded by the ETFA and ETFB genes, respectively. In the present study, we have analysed tissue...

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Source

Identifiers

PMID: 16510302
DOI: 10.1016/j.ymgme.2006.01.009

Genes

ETFA
ETFB
MADD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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