Associated Papers
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance.
Asano T et al.
The Journal of Experimental Medicine, 2021
A Novel STAT3 Mutation in a Qatari Patient With Hyper-IgE Syndrome.
Chaimowitz NS et al.
Frontiers in Pediatrics, 2019
Functional characterization of two new STAT3 mutations associated with hyper-IgE syndrome in a Mexican cohort.
Alcántara-Montiel JC et al.
Clinical Genetics, 2016
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