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Dysregulation of interleukin 5 expression in familial eosinophilia
BACKGROUND: Familial eosinophilia (FE) is a rare autosomal dominant inherited disorder characterized by the presence of lifelong peripheral eosinophilia (>1500/μL). Mapped to chromosome 5q31-q33, the genetic cause of FE is unknown, and prior studies have failed to demonstrate a primary abnormalit...
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| Pubblicato in: | Allergy |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5546948/ https://ncbi.nlm.nih.gov/pubmed/28226398 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/all.13146 |
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