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Rare Mendelian Primary Immunodeficiency diseases associated to impaired NF-κB signaling
Mendelian Primary Immunodeficiency Diseases (MPIDs) are rare disorders affecting distinct constituents of the innate and adaptive immune system. Although they are genetically heterogeneous a substantial group of MPIDs is due to mutations in genes affecting the NF-κB transcription pathway, essential...
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| Publicat a: | Genes Immun |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4457537/ https://ncbi.nlm.nih.gov/pubmed/25764117 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gene.2015.3 |
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