Activating STAT5B mutations can cause both primary hypereosinophilia and lymphocyte-variant hypereosinophilia. uri icon

Overview

publication date

  • October 28, 2022

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

volume

  • 64

issue

  • 1