Associated Papers
Properdin deficiency associated with systemic meningococcal disease due to a novel p.Cys337Arg pathogenic variant.
González-Sánchez L et al.
Genes & Diseases, 2024
Structural Basis for Properdin Oligomerization and Convertase Stimulation in the Human Complement System.
Pedersen DV et al.
Frontiers in Immunology, 2019
Compound heterozygous mutations in IL10RA combined with a complement factor properdin mutation in infantile-onset inflammatory bowel disease.
Jung ES et al.
European Journal of Gastroenterology & Hepatology, 2018
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