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Phosphorylase kinase deficiency: Severe glycogen storage disease with evidence of autosomal recessive mode of inheritance

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References

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Authors and Affiliations

  1. Department of Pediatrics, University of Bergen, 5016 Haukeland Hospital, Bergen, Norway

    O. Søvik

  2. Department of Pathology, University of Bergen, 5016 Haukeland Hospital, Bergen, Norway

    B. Maehle

  3. Laboratoire de Chimie Physiologique, Université Catholique de Louvain, Brussels, Belgium

    Th. de Barsy

Authors
  1. O. Søvik
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  2. Th. de Barsy
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  3. B. Maehle
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Søvik, O., de Barsy, T. & Maehle, B. Phosphorylase kinase deficiency: Severe glycogen storage disease with evidence of autosomal recessive mode of inheritance. Eur J Pediatr 139, 210 (1982). https://doi.org/10.1007/BF01377363

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  • DOI: https://doi.org/10.1007/BF01377363

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