Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.

Benzer Materyaller

• A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease.
  Yazar:: Dinauer, M C, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• 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.
  Yazar:: Dinauer, M C, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)
• Functional defect in neutrophil cytosols from two patients with autosomal recessive cytochrome-positive chronic granulomatous disease.
  Yazar:: Curnutte, J T, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).
  Yazar:: de Boer, M, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• Libyan Boy with Autosomal Recessive Trait (P22-phox Defect) of Chronic Granulomatous Disease
  Yazar:: Al-Bousafy, Ahmed, ve diğerleri
  Baskı/Yayın Bilgisi: (2006)