Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2. (2019)
Attributed to:
Newcastle Confidence in Concept 2016
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1126/sciimmunol.aav7501
PubMed Identifier: 31836668
Publication URI: http://europepmc.org/abstract/MED/31836668
Type: Journal Article/Review
Volume: 4
Parent Publication: Science immunology
Issue: 42
ISSN: 2470-9468