OC1 Clinical and Molecular Features of Twenty Children With Hyper-IgE Syndrome Caused by Stat3 Gene Mutation in Mainland China
doi 10.1136/archdischild-2019-epa.1
Full Text
Open PDFAbstract
Available in full text
Date
June 1, 2019
Authors
Publisher
BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health