Additional file 3 of Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patients

    Dataset

    Description

    Additional file 3: Table S1. Sanger Sequencing HepG2. Results of genotyping WT HepG2 cells and four MCAD-knockouts.
    Date made available4-Sept-2023
    Publisherfigshare

    Keywords on Datasets

    • Medium-chain acyl-CoA dehydrogenase deficiency
    • Mitochondrial fatty acid oxidation
    • Personalised medicine
    • Metabolite partitioning
    • Kinetic modelling
    • Phenotypic heterogeneity
    • Inborn error of metabolism

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