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3-Methylglutaconic aciduria: neonatal onset with lactic acidosis

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Journal of Inherited Metabolic Disease

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References

  • Divry, P., Vianney-Liaud, C., Mory, O. and Ravussin, J. J. 3-Methylglutaconic aciduria: familial neonatal form with fatal onset.J. Inher. Metab. Dis. 10 (1987) 286–289

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  • 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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  • Haan, E. A., Scholem, R. D., Pitt, J. J., Wraith, J. E. and Brown, G. K. Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria.Eur. J. Pediatr. 146 (1987) 484–488

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Authors and Affiliations

  1. Service de Clinique Pédiatrique et Génétique Médicale, CHU, 59037, Lille Cédex, France

    C. Largilliere, B. Cartigny & J. P. Farriaux

  2. Service de Neurologie infantile CHU, 59037, Lille Cédex, France

    L. Vallee & J. P. Nuyts

  3. Service de Néonatologie, CHU, 59037, Lille Cédex, France

    J. P. Dubos

  4. Department of Pediatrics, University of California, La Jolla, USA

    K. M. Gibson

Authors
  1. C. Largilliere
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  2. L. Vallee
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  3. B. Cartigny
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  4. J. P. Dubos
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  5. K. M. Gibson
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  6. J. P. Nuyts
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  7. J. P. Farriaux
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Largilliere, C., Vallee, L., Cartigny, B. et al. 3-Methylglutaconic aciduria: neonatal onset with lactic acidosis. J Inherit Metab Dis 12, 333–334 (1989). https://doi.org/10.1007/BF01799230

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  • DOI: https://doi.org/10.1007/BF01799230

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