IDH
mutations are enriched in myelodysplastic syndrome patients with severe neutropenia and can be a potential for targeted therapy
Haematologica
.
2023 Apr 1;108(4):1168-1172.
doi: 10.3324/haematol.2022.281607.
Authors
Rami Komrokji
1
,
Najla Al Ali
2
,
Onyee Chan
2
,
Kendra Sweet
2
,
Andrew Kuykendall
2
,
Jeffrey Lancet
2
,
Eric Padron
2
,
David A Sallman
2
Affiliations
1
Department of Malignant Hematology, H Lee Moffitt Cancer Center, Tampa, Fl.
[email protected]
.
2
Department of Malignant Hematology, H Lee Moffitt Cancer Center, Tampa, Fl.
PMID:
36420802
PMCID:
PMC10071110
DOI:
10.3324/haematol.2022.281607
No abstract available
Publication types
Letter
MeSH terms
Humans
Isocitrate Dehydrogenase / genetics
Mutation
Myelodysplastic Syndromes* / drug therapy
Myelodysplastic Syndromes* / genetics
Neutropenia* / genetics
Substances
Isocitrate Dehydrogenase