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Familial Hemophagocytic Lymphohistiocytosis due to Mutation of UNC13D Gene
Hemophagocytic lymphohistiocytosis (HLH) are basically a heterogenous group of clinical syndromes, characterised by activation and non-malignant proliferation of benign histiocytes i.e. lymphocytes and macrophages, leading to a cytokine storm that accounts for the fever, organomegaly and multi-organ...
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| Publicat a: | Indian J Hematol Blood Transfus |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer India
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4925480/ https://ncbi.nlm.nih.gov/pubmed/27408432 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-014-0494-x |
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