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Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease
Autoimmune Addison's disease (AAD) is a classic organ-specific autoimmune disease characterized by an immune-mediated attack on the adrenal cortex. As most autoimmune diseases, AAD is believed to be caused by a combination of genetic and environmental factors, and probably interactions between...
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| Publicado no: | J Transl Autoimmun |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7388336/ https://ncbi.nlm.nih.gov/pubmed/32743495 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jtauto.2019.100005 |
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