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

مواد مشابهة

• Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB).
  بواسطة: van den Berg, I E, وآخرون
  منشور في: (1997)
• Families with X linked liver glycogenosis owing to phosphorylase kinase deficiency
  بواسطة: Willems, Patrick
  منشور في: (1990)
• The alpha and beta subunits of phosphorylase kinase are homologous: cDNA cloning and primary structure of the beta subunit.
  بواسطة: Kilimann, M W, وآخرون
  منشور في: (1988)
• I/Lyn mouse phosphorylase kinase deficiency: mutation disrupts expression of the alpha/alpha'-subunit mRNAs.
  بواسطة: Bender, P K, وآخرون
  منشور في: (1989)
• Liver glycogenosis and phosphorylase kinase deficiency.
  بواسطة: Huijing, F, وآخرون
  منشور في: (1970)