Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.

Antzeko izenburuak

• Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
  nork: Dinauer, M C, et al.
  Argitaratua: (1990)
• A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease.
  nork: Dinauer, M C, et al.
  Argitaratua: (1989)
• Identification of a thermolabile component of the human neutrophil NADPH oxidase. A model for chronic granulomatous disease caused by deficiency of the p67-phox cytosolic component.
  nork: Erickson, R W, et al.
  Argitaratua: (1992)
• p47(phox) Phox Homology Domain Regulates Plasma Membrane but Not Phagosome Neutrophil NADPH Oxidase Activation
  nork: Li, Xing Jun, et al.
  Argitaratua: (2010)
• Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).
  nork: de Boer, M, et al.
  Argitaratua: (1992)