학술논문
JAK2 mutation and disease phenotype: a double L611V/V617F in cis mutation of JAK2 is associated with isolated erythrocytosis and increased activation of AKT and ERK1/2 rather than STAT5.
Document Type
Letter
Author
Source
Subject
*LETTERS to the editor
*GENETIC mutation
*
Language
ISSN
0887-6924
Abstract
A letter to the editor is presented related to mutations in patients with myeloproliferative neoplasm.