An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis
Institute for Rheumatic Diseases (Japan) · RIKEN · +2 more institutions
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Abstract
No abstract available for this paper.
Citation impact
641
total citations
- FWCI
- 40.18
- Percentile
- 100%
- References
- 46
Citations per year
Authors
20- STShinya TokuhiroCorresponding
Institute for Rheumatic Diseases (Japan), RIKEN
- RYRyo Yamada
RIKEN, Institute for Rheumatic Diseases (Japan)
- XCXiaotian Chang
Institute for Rheumatic Diseases (Japan), RIKEN
- ASAkari Suzuki
RIKEN, Institute for Rheumatic Diseases (Japan)
- YKYuta Kochi
RIKEN, Institute for Rheumatic Diseases (Japan), The University of Tokyo
Topics & keywords
Topics
Keywords
- Single-nucleotide polymorphism
- Linkage disequilibrium
- Arthritis
- Rheumatoid arthritis
- Biology
- RUNX1
- Genetics
- SNP
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