Association of the PTPN22 C1858T single-nucleotide polymorphism with rheumatoid arthritis phenotypes in an inception cohort

Arthritis Rheum. 2005 Sep;52(9):2948-50. doi: 10.1002/art.21294.

Authors

J Wesoly¹, A H M van der Helm-van Mil, R E Toes, A P Chokkalingam, V E H Carlton, A B Begovich, T W J Huizinga

Affiliation

¹ Leiden University Medical Center, Leiden, The Netherlands.

PMID: 16145680
DOI: 10.1002/art.21294

No abstract available

MeSH terms

Arthritis, Rheumatoid / diagnosis
Arthritis, Rheumatoid / epidemiology
Arthritis, Rheumatoid / genetics*
Arthrography
Cohort Studies
Early Diagnosis
Gene Frequency
Genetic Predisposition to Disease*
Humans
Joints / pathology
Mutation, Missense*
Netherlands / epidemiology
Phenotype
Polymorphism, Single Nucleotide*
Protein Tyrosine Phosphatase, Non-Receptor Type 22
Protein Tyrosine Phosphatases / genetics*
Severity of Illness Index

Substances

PTPN22 protein, human
Protein Tyrosine Phosphatase, Non-Receptor Type 22
Protein Tyrosine Phosphatases