IL1RN genotype as a risk factor for joint pain in hereditary haemochromatosis?

Annals of the Rheumatic Diseases

Volumn 65, Issue 2, 2006, Pages 271-272

  Walker, E J ^a   Riddell, J ^b   Rodgers, H J ^b   Bassett, M L ^b   Wilson, S R ^c   Cavanaugh, J A ^b  

^a Australian National University   (Australia)

^b CANBERRA HOSPITAL   (Australia)

^c AUSTRALIAN NATIONAL UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FERRITIN; INTERLEUKIN 1 RECEPTOR;

ALLELE; ARTHRALGIA; ARTHRITIS; ARTICLE; CHROMOSOME 2; CONTROLLED STUDY; CORRELATION ANALYSIS; DNA EXTRACTION; ENZYME LINKED IMMUNOSORBENT ASSAY; FEMALE; FERRITIN BLOOD LEVEL; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENOTYPE; HEMOCHROMATOSIS; HOMOZYGOTE; HUMAN; IL1RN GENE; IRON OVERLOAD; IRON STORAGE; MAJOR CLINICAL STUDY; MALE; OSTEOARTHRITIS; PRIORITY JOURNAL; RISK FACTOR;

ALLELES; ARTHRALGIA; CASE-CONTROL STUDIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HEMOCHROMATOSIS; HUMANS; MALE; RECEPTORS, INTERLEUKIN-1;

EID: 31144453914     PISSN: 00034967     EISSN: None     Source Type: Journal    
DOI: 10.1136/ard.2005.038158     Document Type: Article

References (10)

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