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Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Emery, J. L., Howat, A. J., Variend, S. and Vawter, G. F. Investigation of inborn errors of metabolism in unexpected infant deaths.Lancet 1 (1988) 29–31

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  • Gibson, K. M., Breuer, J. and Nyhan, W. L. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients.Eur. J. Pediatr. 148 (1988) 180–186

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  • Wysocky, S. J. and Hähnel, R. 3-Hydroxy-3-methylglutaric aciduria: 3-hydroxy-3-methylglutaryl-coenzyme A lyase levels in leukocytes.Clin. Chim. Acta 73 (1976) 373–375

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Authors and Affiliations

  1. Institut de Bioquímica Clínica, Diputació de Barcelona, Apartat de Correus 137, 08290, Cerdanyola, Barcelona, Spain

    A. Ribes & M. A. Vilaseca

  2. Department de Bioquímica Clínica, CSIC, Cerdanyola, Barcelona, Spain

    P. Briones

  3. Departament de Pediatria, Institut Dexeus, Barcelona, Spain

    R. Baraibar & J. M. Gairi

Authors
  1. A. Ribes
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  2. P. Briones
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  3. M. A. Vilaseca
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  4. R. Baraibar
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  5. J. M. Gairi
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Ribes, A., Briones, P., Vilaseca, M.A. et al. Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency. J Inherit Metab Dis 13, 752–753 (1990). https://doi.org/10.1007/BF01799579

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  • DOI: https://doi.org/10.1007/BF01799579

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