A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease.

समान संसाधन

• Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
  द्वारा: Dinauer, M C, और अन्य
  प्रकाशित: (1990)
• Functional defect in neutrophil cytosols from two patients with autosomal recessive cytochrome-positive chronic granulomatous disease.
  द्वारा: Curnutte, J T, और अन्य
  प्रकाशित: (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.
  द्वारा: Dinauer, M C, और अन्य
  प्रकाशित: (1991)
• Mutations in the promoter region of the gene for gp91-phox in X-linked chronic granulomatous disease with decreased expression of cytochrome b558.
  द्वारा: Newburger, P E, और अन्य
  प्रकाशित: (1994)
• Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b.
  द्वारा: Parkos, C A, और अन्य
  प्रकाशित: (1988)