Therapeutic options in VEXAS syndrome: insights from a retrospective series.
Blood
; 137(26): 3682-3684, 2021 07 01.
Article
in En
| MEDLINE
| ID: mdl-33619558
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Mutation, Missense
/
Ubiquitin-Activating Enzymes
/
Genetic Diseases, Inborn
/
Mutation
/
Myeloproliferative Disorders
Limits:
Humans
Language:
En
Journal:
Blood
Year:
2021
Type:
Article