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RAG gene defects at the verge of immunodeficiency and immune dysregulation
Mutations of the Recombinase Activating Genes (RAG) in humans underlie a broad spectrum of clinical and immunological phenotypes that reflect different degrees of impairment of T and B cell development and alterations of mechanisms of central and peripheral tolerance. Recent studies have shown that...
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| Publicado no: | Immunol Rev |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6309314/ https://ncbi.nlm.nih.gov/pubmed/30565244 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/imr.12713 |
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