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3-Methylglutaconic aciduria with persistent metabolic acidosis and ‘uncoupling episodes’

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Gibson, K. M., Nyhan, W. L., Sweetman, L., Narisawa, K., Lehnert, W., Divry, P., Robinson, B. H., Roth, K. S., Beemer, F. A., van Sprang, F. J., Duran, M., Wadman, S. K. and Cartigny, B. 3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal.Eur. J. Pediatr. 148 (1988) 76–82

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Authors and Affiliations

  1. Department of Pediatrics and Neuropediatrics, Bikur-Cholim Hospital, Jerusalem, Israel

    O. N. Elpeleg & N. Amir

  2. Department of Pediatrics A, Central Emek Hospital, Afula, Israel

    D. Meiron, Y. Hurwitz & I. Tal

  3. Department of Clinical Biochemistry, Hadassah Hospital, Jerusalem, Israel

    V. Barash

Authors
  1. O. N. Elpeleg
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  2. D. Meiron
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  3. V. Barash
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  4. Y. Hurwitz
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  5. I. Tal
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  6. N. Amir
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Elpeleg, O.N., Meiron, D., Barash, V. et al. 3-Methylglutaconic aciduria with persistent metabolic acidosis and ‘uncoupling episodes’. J Inherit Metab Dis 13, 235–236 (1990). https://doi.org/10.1007/BF01799695

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  • DOI: https://doi.org/10.1007/BF01799695

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