Functional defect in neutrophil cytosols from two patients with autosomal recessive cytochrome-positive chronic granulomatous disease.

Lignende værker

• A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease.
  af: Dinauer, M C, et al.
  Udgivet: (1989)
• Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
  af: Dinauer, M C, et al.
  Udgivet: (1990)
• Cytosolic components of the respiratory burst oxidase: resolution of four components, two of which are missing in complementing types of chronic granulomatous disease.
  af: Curnutte, J T, et al.
  Udgivet: (1989)
• Libyan Boy with Autosomal Recessive Trait (P22-phox Defect) of Chronic Granulomatous Disease
  af: Al-Bousafy, Ahmed, et al.
  Udgivet: (2006)
• Chronic granulomatous disease due to a defect in the cytosolic factor required for nicotinamide adenine dinucleotide phosphate oxidase activation.
  af: Curnutte, J T, et al.
  Udgivet: (1988)