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.
Authors
O Søvik
,
T deBarsy
,
B Maehle
PMID:
6962066
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