RUNX1 intronic SNP is not associated with rheumatoid arthritis susceptibility in Dutch Caucasians [1]

Rheumatology

Volumn 44, Issue 9, 2005, Pages 1196-

  Wesoly, J ^a   Toes, R E M ^a   Slagboom, P E ^a   Huizinga, T W J ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR RUNX1;

CAUCASIAN; CHI SQUARE TEST; CONTROLLED STUDY; DISEASE PREDISPOSITION; GENE FREQUENCY; GENOTYPE; HUMAN; LETTER; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; RHEUMATOID ARTHRITIS; SINGLE NUCLEOTIDE POLYMORPHISM; TIME OF FLIGHT MASS SPECTROMETRY;

ARTHRITIS, RHEUMATOID; CORE BINDING FACTOR ALPHA 2 SUBUNIT; DNA-BINDING PROTEINS; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTO-ONCOGENE PROTEINS; TRANSCRIPTION FACTORS;

EID: 24144493060     PISSN: 14620324     EISSN: None     Source Type: Journal    
DOI: 10.1093/rheumatology/kei009     Document Type: Letter

References (4)

1. Tokuhiro S, Yamada R, Chang X et al. An intronic SNP in RUNX1 binding site of SLC22A4 encoding an organic cation transporter is associated with rheumatoid arthritis. Nat Genet 2003;35:341-8.
2. van Aken J, van Bilsen JH, Allart CF, Huizinga TW, Breedveld FC. The Leiden Early Arthritis Clinic. Clin Exp Rheumatol 2003; 21(5 Suppl. 31):S100-5.
3. Brinkman BM, Huizinga TW, Kurban SS, van der Velde EA. Tumour necrosis factor alpha gene polymorphisms in rheumatoid arthritis: Association with susceptibility to, or severity of, disease? Br J Rheumatol 1997;36:516-21.
4. Butt C, Sun S, Greenwood C, Gladman D, Rahman P. Lack of association of SLC22A4, SLC22A5, SLC9A3R1 and RUNX1 variants in psoriatic arthritis. Rheumatology 2005;44:820-1.