JAK2V617F mutation can occur exclusively in the erythroid lineage and be absent in granulocytes and progenitor cells in classic myeloproliferative disorders

Subjects

Subjects :

Genetics
Myeloproliferative Disorders
Janus kinase 2
Lineage (genetic)
biology
medicine.diagnostic_test
Stem Cells
Point mutation
DNA Mutational Analysis
Hematology
Janus Kinase 2
Flow Cytometry
Molecular biology
Flow cytometry
Erythroid Cells
biology.protein
medicine
Humans
Point Mutation
Cell Lineage
Progenitor cell
Stem cell
Granulocytes

Details

ISSN :

10968652 and 03618609

Volume :

81

Database :

OpenAIRE

Journal :

American Journal of Hematology

Accession number :

edsair.doi.dedup.....a59b4f53653eb9ee4c644467fcd2dd11

Full Text :

https://doi.org/10.1002/ajh.20663