Unmasking NCF1 Gene Defects: Atypical Presentations of p47phox Deficiency in Chronic Granulomatous Disease Article

Budhu, Gail, Kuhns, Douglas, Davis, Joie et al. (2025). Unmasking NCF1 Gene Defects: Atypical Presentations of p47phox Deficiency in Chronic Granulomatous Disease . Journal of human immunity, 1(CIS2025), 10.70962/cis2025abstract.92

cited authors

  • Budhu, Gail; Kuhns, Douglas; Davis, Joie; Holland, Steven; Ale, Hanadys

authors

publication date

  • April 25, 2025

published in

keywords

  • 2.1 Biological and endogenous factors
  • 31 Biological Sciences
  • 32 Biomedical and Clinical Sciences
  • 3202 Clinical Sciences
  • Genetics
  • Human Genome
  • Pediatric Research Initiative
  • Rare Diseases

Digital Object Identifier (DOI)

publisher

  • Rockefeller University Press

volume

  • 1

issue

  • CIS2025