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The role of PTPN22 risk variant in the development of autoimmunity: Finding common ground between mouse and man
The PTPN22 1858T variant was among the first single nucleotide polymorphisms (snp) to be associated with multiple autoimmune diseases. As a coding variant within the tyrosinephosphatase, Lyp, known to participate in antigen receptor signaling, the impact of this variant on the immune response and ro...
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| Publicat a: | J Immunol |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4369788/ https://ncbi.nlm.nih.gov/pubmed/25795788 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4049/jimmunol.1403034 |
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