Abstract
Glutaric acidemia type II is a human inborn error of metabolism which can be due to defects in either subunit of electron transfer flavoprotein (ETF) or in ETF:ubiquinone oxidoreductase (ETF:QO), but few disease-causing mutations have been described. The ETF:QO gene is located on 4q33, and contains 13 exons. Primers to amplify these exons are presented, together with mutations identified by molecular analysis of 20 ETF:QO-deficient patients. Twenty-one different disease-causing mutations were identified on 36 of the 40 chromosomes.
MeSH terms
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Amino Acid Metabolism, Inborn Errors / blood
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Amino Acid Metabolism, Inborn Errors / enzymology*
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Amino Acid Metabolism, Inborn Errors / genetics*
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Base Sequence
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DNA Mutational Analysis
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DNA, Complementary / genetics
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Electron-Transferring Flavoproteins*
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Exons
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Fatty Acid Desaturases / deficiency*
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Fatty Acid Desaturases / genetics*
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Genotype
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Glutarates / blood*
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Humans
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Introns
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Iron-Sulfur Proteins*
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Lipid Metabolism, Inborn Errors / blood
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Lipid Metabolism, Inborn Errors / enzymology*
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Lipid Metabolism, Inborn Errors / genetics*
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Multienzyme Complexes / deficiency*
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Multienzyme Complexes / genetics*
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Mutation*
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Oxidoreductases Acting on CH-NH Group Donors*
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Phenotype
Substances
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DNA, Complementary
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Electron-Transferring Flavoproteins
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Glutarates
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Iron-Sulfur Proteins
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Multienzyme Complexes
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Fatty Acid Desaturases
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Oxidoreductases Acting on CH-NH Group Donors
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electron-transferring-flavoprotein dehydrogenase
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glutaric acid