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Literature summary for 1.5.5.1 extracted from

  • Wu, Y; Han, J; Wang, Y; Zhang, J; Song, X; Ji, G
    A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene. (2020), J Int Med Res, 48, 300060520966499.
    View publication on PubMedView publication on EuropePMC
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Organism

Organism UniProt Comment Textmining