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Haematopoietic and immune defects associated with GATA2 mutation
Heterozygous familial or sporadic GATA2 mutations cause a multifaceted disorder, encompassing susceptibility to infection, pulmonary dysfunction, autoimmunity, lymphoedema and malignancy. Although often healthy in childhood, carriers of defective GATA2 alleles develop progressive loss of mononuclear...
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| Опубликовано в: : | Br J Haematol |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Blackwell Publishing Ltd
2015
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4409096/ https://ncbi.nlm.nih.gov/pubmed/25707267 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bjh.13317 |
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