Abstracts 2019
DOI: 10.1136/archdischild-2019-epa.1
|View full text |Cite
|
Sign up to set email alerts
|

OC1 Clinical and molecular features of twenty children with hyper-IgE syndrome caused by stat3 gene mutation in mainland china

Help me understand this report

This publication either has no citations yet, or we are still processing them

Set email alert for when this publication receives citations?

See others like this or search for similar articles