Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
收藏NIAID Data Ecosystem2026-03-12 收录
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Here we describe patients with an autosomal recessive form of HIES due to loss-of-function mutations of a previously uncharacterized gene, ZNF341. Examination of gene expression in EBV-B cells from healthy and ZNF341 patients stimulated with IL-21, IL-6, IL-23, IL-10, and IFNa
创建时间：
2021-06-13
