Casanova J, Abel L
Annu Rev Pathol. 2020; 16:23-50.
PMID: 32289233
PMC: 7923385.
DOI: 10.1146/annurev-pathol-031920-101429.
Lo M
Front Immunol. 2018; 9:1278.
PMID: 29922296
PMC: 5996073.
DOI: 10.3389/fimmu.2018.01278.
Lo M
Curr Rheumatol Rep. 2016; 18(12):71.
PMID: 27812953
DOI: 10.1007/s11926-016-0621-9.
Jiang W, Gilkeson G
J Immunother Appl. 2014; 1:1.
PMID: 25309746
PMC: 4193900.
DOI: 10.7243/2055-2394-1-1.
Ramos P, Shaftman S, Ward R, Langefeld C
Autoimmune Dis. 2014; 2014:203435.
PMID: 24587899
PMC: 3920976.
DOI: 10.1155/2014/203435.
Complement genetics, deficiencies, and disease associations.
Mayilyan K
Protein Cell. 2012; 3(7):487-96.
PMID: 22773339
PMC: 4875391.
DOI: 10.1007/s13238-012-2924-6.
Genetics of Sjögren's syndrome in the genome-wide association era.
Ice J, Li H, Adrianto I, Lin P, Kelly J, Montgomery C
J Autoimmun. 2012; 39(1-2):57-63.
PMID: 22289719
PMC: 3518871.
DOI: 10.1016/j.jaut.2012.01.008.
Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis.
Ramos P, Brown E, Kimberly R, Langefeld C
Semin Nephrol. 2010; 30(2):164-76.
PMID: 20347645
PMC: 2847514.
DOI: 10.1016/j.semnephrol.2010.01.007.
Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.
de Smith A, Walters R, Froguel P, Blakemore A
Cytogenet Genome Res. 2009; 123(1-4):17-26.
PMID: 19287135
PMC: 2920180.
DOI: 10.1159/000184688.
Immunoglobulin deficiencies and susceptibility to infection among homozygotes and heterozygotes for C2 deficiency.
Alper C, Xu J, Cosmopoulos K, Dolinski B, Stein R, Uko G
J Clin Immunol. 2003; 23(4):297-305.
PMID: 12959222
DOI: 10.1023/a:1024540917593.
Hereditary deficiency of the sixth component of complement in man. I. Immunochemical, biologic, and family studies.
Leddy J, Frank M, Gaither T, Baum J, KLEMPERER M
J Clin Invest. 1974; 53(2):544-53.
PMID: 11344568
PMC: 301497.
DOI: 10.1172/JCI107588.
Recurrent pyogenic infections in individuals with absence of the second component of complement.
Sampson H, Walchner A, Baker P
J Clin Immunol. 1982; 2(1):39-45.
PMID: 6980226
DOI: 10.1007/BF00915977.
Meningococcal meningitis associated with persistent hypocomplementaemia due to circulating C3 nephritic factor.
Thompson R, Yap P, Brettle R, Dunmow R, Chapel H
Clin Exp Immunol. 1983; 52(1):153-6.
PMID: 6861372
PMC: 1535563.
Partial H (beta 1H) deficiency and glomerulonephritis in two families.
Wyatt R, Julian B, Weinstein A, Rothfield N, McLean R
J Clin Immunol. 1982; 2(2):110-7.
PMID: 6461667
DOI: 10.1007/BF00916894.
Inherited deficiencies of complement proteins in man.
Alper C, Rosen F
Springer Semin Immunopathol. 1984; 7(2-3):251-61.
PMID: 6238435
DOI: 10.1007/BF01893022.
Serum factors responsible for killing of Shigella.
REED W, Albright E
Immunology. 1974; 26(1):205-15.
PMID: 4846468
PMC: 1423117.
Deficiency of the second component of complement associated with anaphylactoid purpura and presence of mycoplasma in the serum.
Sussman M, Jones J, Almeida J, LACHMANN P
Clin Exp Immunol. 1973; 14(4):531-9.
PMID: 4583776
PMC: 1553813.
C2 deficiency. Development of lupus erythematosus.
Day N, Geiger H, McLean R, Michael A, GOOD R
J Clin Invest. 1973; 52(7):1601-7.
PMID: 4578155
PMC: 302431.
DOI: 10.1172/JCI107337.
The immunological basis of glomerulonephritis.
PETERS D
Proc R Soc Med. 1974; 67(6 Pt 2):557-62.
PMID: 4369312
PMC: 1645576.
The autosomal recessive mode of inheritance of C1r deficiency in a large Puerto Rican family.
De Bracco M, WINDHORST D, Stroud R, Moncada B
Clin Exp Immunol. 1974; 16(2):183-8.
PMID: 4219876
PMC: 1553918.