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Identifying functional defects in patients with immune dysregulation due to LRBA and CTLA-4 mutations
Heterozygous CTLA-4 deficiency has been reported as a monogenic cause of common variable immune deficiency with features of immune dysregulation. Direct mutation in CTLA-4 leads to defective regulatory T-cell (Treg) function associated with impaired ability to control levels of the CTLA-4 ligands, C...
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| Publicado no: | Blood |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Hematology
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5438243/ https://ncbi.nlm.nih.gov/pubmed/28159733 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2016-10-745174 |
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