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3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency

  • Case Report
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Journal of Inherited Metabolic Disease

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References

  • Faull, K., Bolton, P., Halpern, B., Hammond, J., Danks, D. M., Hahnel, R., Wilkinson, S. P., Wysocki, S. J. and Masters, P. L. Patient with defect in leucine metabolism.N. Engl. J. Med. 294 (1976) 1013

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Authors and Affiliations

  1. Departments of Pediatrics, Soroka Medical Center, Ben Gurion University, Beersheva

    S. W. Moses & M. Aviram

  2. Poriah Hospital, Tiberias, Israel

    R. Geiger

  3. University of Groningen, The Netherlands

    R. Berger & P. C. Smit

Authors
  1. S. W. Moses
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  2. M. Aviram
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  3. R. Geiger
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  4. R. Berger
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  5. P. C. Smit
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Moses, S.W., Aviram, M., Geiger, R. et al. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency. J Inherit Metab Dis 12, 341–342 (1989). https://doi.org/10.1007/BF01799235

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  • DOI: https://doi.org/10.1007/BF01799235

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