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

Ítems similars

• Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
  per: Dinauer, M C, et al.
  Publicat: (1990)
• Functional defect in neutrophil cytosols from two patients with autosomal recessive cytochrome-positive chronic granulomatous disease.
  per: Curnutte, J T, et al.
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• 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.
  per: Dinauer, M C, et al.
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  per: Newburger, P E, et al.
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• Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b.
  per: Parkos, C A, et al.
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