X-chromosomal inheritance of liver glycogenosis with phosphorylase kinase deficiency

Am J Hum Genet. 1969 May;21(3):275-84.
No abstract available

MeSH terms

  • Adenine Nucleotides / blood
  • Adolescent
  • Adult
  • Aged
  • Child
  • Child, Preschool
  • Chromosome Aberrations*
  • Chromosome Disorders*
  • Color Vision Defects / genetics
  • Crossing Over, Genetic
  • Erythrocytes
  • Female
  • Glucosyltransferases / blood
  • Glycogen Storage Disease / genetics*
  • Heterozygote
  • Humans
  • Infant
  • Infant, Newborn
  • Leukocytes / enzymology
  • Male
  • Metabolism, Inborn Errors / complications*
  • Methods
  • Middle Aged
  • Pedigree
  • Phosphorylase Kinase / blood
  • Phosphorylase Kinase / metabolism*
  • Sex Chromosomes*

Substances

  • Adenine Nucleotides
  • Glucosyltransferases
  • Phosphorylase Kinase