Mannose-binding lectin-low genotypes are associated with milder systemic and immunological disease expression in primary Sjögren's syndrome

Rheumatology

Volumn 48, Issue 1, 2009, Pages 65-69

  Ramos Casals, M ^a   Brito Zeron P ^a   Soria, N ^a   Nardi, N ^a   Vargas, A ^a   Munoz S ^a   Bove A ^a   Suarez B ^a   Lozano, F ^a  

^a HOSPITAL CLÍNIC   (Spain)

Author keywords

Anti Ro SS A antibodies; Gene polymorphism; Innate immunity; Mannose binding lectin; Primary Sj gren's syndrome

Indexed keywords

COMPLEMENT COMPONENT C3; COMPLEMENT COMPONENT C4; CRYOGLOBULIN; LA ANTIBODY; MANNOSE BINDING LECTIN 2; RO ANTIBODY;

ADULT; ANTIBODY BLOOD LEVEL; ANTIBODY DETECTION; ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; DNA FINGERPRINTING; EXON; FEMALE; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENOTYPE; GLOMERULONEPHRITIS; HOMOZYGOTE; HUMAN; IMMUNOPATHOLOGY; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; NEUROLOGIC DISEASE; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN BLOOD LEVEL; PURPURA; SEQUENCE ANALYSIS; SJOEGREN SYNDROME; SYSTEMIC DISEASE; SYSTEMIC LUPUS ERYTHEMATOSUS;

AUTOANTIBODIES; AUTOANTIGENS; BIOLOGICAL MARKERS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; IMMUNITY, INNATE; MALE; MANNOSE-BINDING LECTIN; MANNOSE-BINDING PROTEIN-ASSOCIATED SERINE PROTEASES; MIDDLE AGED; POLYMORPHISM, GENETIC; RETROSPECTIVE STUDIES; RIBONUCLEOPROTEINS; RNA, SMALL CYTOPLASMIC; SJOGREN'S SYNDROME;

EID: 57349102250     PISSN: 14620324     EISSN: 14620332     Source Type: Journal    
DOI: 10.1093/rheumatology/ken411     Document Type: Article

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