Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22

This publication has 16 references indexed in Scilit:

• Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome
  Cytogenetic and Genome Research, 1990
• Report of the committee on linkage and gene order
  Cytogenetic and Genome Research, 1989
• Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3)
  Cytogenetic and Genome Research, 1989
• X-Linked genetic homologies between mouse and man
  Genomics, 1987
• Isolation and sequence analysis of a cDNA clone encoding the entire catalytic subunit of phosphorylase kinase
  FEBS Letters, 1987
• The autosomal form of phosphorylase kinase defficiency in man: Reduced activity of the muscle enzyme
  Biochemical and Biophysical Research Communications, 1980
• The Molecular Basis of Skeletal Muscle Phosphorylase Kinase Deficiency
  European Journal of Biochemistry, 1976
• Glycogen storage disease type IX: Benign glycogenosis of liver and hepatic phosphorylase kinase deficiency
  The Journal of Pediatrics, 1973
• Glycogen phosphorylase kinase deficiency: A survey of enzymes in phosphorylase activating system
  Biochemical and Biophysical Research Communications, 1973
• Phosphorylase kinase in leucocytes of normal subjects and of patients with glycogen-storage disease
  Biochimica et Biophysica Acta (BBA) - General Subjects, 1967