Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridization.

مواد مشابهة

• Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridization
  منشور في: (1985)
• Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).
  بواسطة: de Boer, M, وآخرون
  منشور في: (1992)
• Hematologically Important Mutations: The Autosomal Recessive Forms of Chronic Granulomatous Disease (Second Update)
  بواسطة: Roos, Dirk, وآخرون
  منشور في: (2010)
• Molecular diagnosis of chronic granulomatous disease
  بواسطة: Roos, D, وآخرون
  منشور في: (2014)
• A phosphoprotein of Mr 47,000, defective in autosomal chronic granulomatous disease, copurifies with one of two soluble components required for NADPH:O2 oxidoreductase activity in human neutrophils.
  بواسطة: Bolscher, B G, وآخرون
  منشور في: (1989)