Open AccessP777: RUNX1 VARIANTS WITH HIGH VARIANT ALLELE FREQUENCY IN MYELOID NEOPLASMS. GERMLINE OR NOT?
Author(s) -
Nitschke N. J.,
Krogh M.,
RaaschouJensen K.,
Severinsen M. T.,
Roug A. S.,
Jespersen J. S.,
Hansen J. W.,
Weischenfeldt J.,
Andersen M. K.,
Grønbæk K.
Publication year - 2022
Publication title -
hemasphere
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 11
ISSN - 2572-9241
DOI - 10.1097/01.hs9.0000845992.27176.7c
Subject(s) - germline , frameshift mutation , runx1 , myeloid leukemia , germline mutation , biology , platelet disorder , sanger sequencing , genetics , myeloid , missense mutation , cancer research , mutation , immunology , gene , platelet , transcription factor