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Association between PTPN22 C1858T polymorphism and alopecia areata risk
Alopecia areata (AA) is a skin condition in which hair is lost from certain or all areas of the body. This condition has been described as an immune-mediated complex genetic disease, characterized by the presence of lymphocytes that are directed to the hair follicles in the anagen phase. The gene en...
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| Publicat a: | Exp Ther Med |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
D.A. Spandidos
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4665763/ https://ncbi.nlm.nih.gov/pubmed/26640579 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2015.2728 |
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