Novel somatic mutations in UBA1 as a cause of VEXAS syndrome. (2021)
Attributed to:
Characterising and targeting Cyclin D stabilisation in development and disease.
funded by
FLF
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1182/blood.2020010286
PubMed Identifier: 33690815
Publication URI: http://europepmc.org/abstract/MED/33690815
Type: Journal Article/Review
Volume: 137
Parent Publication: Blood
Issue: 26
ISSN: 0006-4971