European Journal of Pediatrics

, Volume 139, Issue 3, pp 210–210

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

Authors

  • O. Søvik
    • Department of PediatricsUniversity of Bergen, 5016 Haukeland Hospital
  • Th. de Barsy
    • Laboratoire de Chimie PhysiologiqueUniversité Catholique de Louvain
  • B. Maehle
    • Department of PathologyUniversity of Bergen, 5016 Haukeland Hospital
Letters to the Editors

DOI: 10.1007/BF01377363

Cite this article as:
Søvik, O., de Barsy, T. & Maehle, B. Eur J Pediatr (1982) 139: 210. doi:10.1007/BF01377363

Copyright information

© Springer-Verlag 1982