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

Eur J Pediatr. 1982 Nov;139(3):210. doi: 10.1007/BF01377363.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Female
  • Glycogen Storage Disease / etiology*
  • Humans
  • Infant
  • Phosphorylase Kinase / deficiency*

Substances

  • Phosphorylase Kinase