SETBP1 mutations in 415 patients with primary myelofibrosis or chronic myelomonocytic leukemia: independent prognostic impact in CMML

Leukemia. 2013 Oct;27(10):2100-2. doi: 10.1038/leu.2013.97. Epub 2013 Apr 5.

Authors

R R Laborde¹, M M Patnaik, T L Lasho, C M Finke, C A Hanson, R A Knudson, R P Ketterling, A Pardanani, A Tefferi

Affiliation

¹ Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN, USA.

No abstract available

Publication types

Letter

MeSH terms

Aged
Carrier Proteins / genetics*
DNA Mutational Analysis
Female
Follow-Up Studies
Humans
Leukemia, Myelomonocytic, Chronic / genetics*
Leukemia, Myelomonocytic, Chronic / mortality
Male
Mutation / genetics*
Nuclear Proteins / genetics*
Primary Myelofibrosis / genetics*
Primary Myelofibrosis / mortality
Prognosis
RNA, Messenger / genetics
Real-Time Polymerase Chain Reaction
Reverse Transcriptase Polymerase Chain Reaction
Survival Rate

Substances

Carrier Proteins
Nuclear Proteins
RNA, Messenger
SETBP1 protein, human