X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunit.

Liknande verk

• Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB).
  av: van den Berg, I E, et al.
  Publicerad: (1997)
• The alpha and beta subunits of phosphorylase kinase are homologous: cDNA cloning and primary structure of the beta subunit.
  av: Kilimann, M W, et al.
  Publicerad: (1988)
• cDNA cloning and complete primary structure of skeletal muscle phosphorylase kinase (alpha subunit).
  av: Zander, N F, et al.
  Publicerad: (1988)
• Families with X linked liver glycogenosis owing to phosphorylase kinase deficiency
  av: Willems, Patrick
  Publicerad: (1990)
• Activation and phosphorylation of the subunits of phosphorylase kinase.
  av: Cohen, P
  Publicerad: (1972)