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Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?

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Journal of Inherited Metabolic Disease

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Authors and Affiliations

  1. Hôpital Enfants-Malades, Clinique Génétique Médicale, 149 rue de Sèvres, 75015, Paris, France

    B. T. Poll-The, J. P. Bonnefont, H. Ogier, C. Charpentier, A. Pelet & J. M. Saudubray

  2. CHU Augustin-Morvan, Brest, France

    J. M. Le Fur

  3. Free University of Amsterdam, Amsterdam, The Netherlands

    C. Jakobs & R. M. Kok

  4. University Children's Hospital “Het Wilhelmina Kinderziekenhuis”, Utrecht, The Netherlands

    M. Duran

  5. Hôpital Debrousse, Lyon, France

    P. Divry

  6. Hôpital Bicêtre et INSERM U 56, Paris, France

    J. Scotto

Authors
  1. B. T. Poll-The
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  2. J. P. Bonnefont
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  3. H. Ogier
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  4. C. Charpentier
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  5. A. Pelet
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  6. J. M. Le Fur
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  7. C. Jakobs
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  8. R. M. Kok
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  9. M. Duran
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  10. P. Divry
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  11. J. Scotto
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  12. J. M. Saudubray
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Poll-The, B.T., Bonnefont, J.P., Ogier, H. et al. Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?. J Inherit Metab Dis 11 (Suppl 2), 183–185 (1988). https://doi.org/10.1007/BF01804230

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  • DOI: https://doi.org/10.1007/BF01804230

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