Llwytho...
The association of the PTPN22 620W polymorphism with Behçet's disease
OBJECTIVES: A single nucleotide polymorphism (SNP) of the gene encoding protein tyrosine phosphatase type 22 (PTPN22 620W) has recently been described as a strong common genetic risk factor for human autoimmune disease. We have analysed the association of PTPN22 620W in patients with Behçet's d...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BMJ Group
2007
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2111602/ https://ncbi.nlm.nih.gov/pubmed/17660222 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/ard.2007.073866 |
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