📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Novel somatic mutations in UBA1 as a cause of VEXAS syndrome. (2021)

First Author: Poulter JA

Attributed to: Characterising and targeting Cyclin D stabilisation in development and disease. funded by UKRI 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