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September 1, 1994Journal of Clinical InvestigationOpen Access

Mutations in the promoter region of the gene for gp91-phox in X-linked chronic granulomatous disease with decreased expression of cytochrome b558.

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Authors

Peter E. Newburger
Peter E. NewburgerUniversity of Massachusetts Chan Medical SchoolDSDavid G. SkalnikIndiana University – Purdue University IndianapolisPHPenelope J. HopkinsCredo Reference (United States)

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Newburger et al. (1994) studied this question.

synapsesocial.com/papers/6aa561f85175d8ad94396282https://doi.org/10.1172/jci117437
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Also Consider

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  1. 1Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer.1988 · 4,635 citations
  2. 2Characterization of a new human diploid myeloid leukemia cell line (PLB- 985) with granulocytic and monocytic differentiating capacity1987 · 223 citations
  3. 3B cell lines as models for inherited phagocytic diseases: abnormal superoxide generation in chronic granulomatous disease and giant granules in Chediak-Higashi syndrome.1984 · 130 citations
  4. 4Point mutations in the beta-subunit of cytochrome b558 leading to X- linked chronic granulomatous disease1991 · 113 citations