Activating STAT5B mutations can cause both primary hypereosinophilia and lymphocyte-variant hypereosinophilia.
Overview
publication date
- October 28, 2022
published in
- Leukemia & lymphoma Journal
Research
keywords
- Hypereosinophilic Syndrome
Identity
PubMed Central ID
- PMC11026062
Scopus Document Identifier
- 85141137715
Digital Object Identifier (DOI)
- 10.1080/10428194.2022.2131413
PubMed ID
- 36308018
Additional Document Info
has global citation frequency
volume
- 64
issue
- 1