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WHIM Syndrome: from Pathogenesis towards Personalized Medicine and Cure
WHIM syndrome is a rare combined primary immunodeficiency disease named by acronym for the diagnostic tetrad of Warts, Hypogammaglobulinemia, Infections and Myelokathexis. Myelokathexis is a unique form of non-cyclic severe congenital neutropenia caused by accumulation of mature and degenerating neu...
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| Publicat a: | J Clin Immunol |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6698215/ https://ncbi.nlm.nih.gov/pubmed/31313072 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10875-019-00665-w |
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