Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosis

International IBD Genetics Consortium

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)
Original languageEnglish
Article number329689
JournalGut
DOIs
Publication statusAccepted/In press - 2023

ASJC Scopus Subject Areas

  • Gastroenterology

Keywords

  • IBD - GENETICS
  • INFLAMMATORY BOWEL DISEASE
  • META-ANALYSIS

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