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Driver mutation‐specific clinical and genomic correlates differ between primary and secondary myelofibrosis
Author(s) -
Kuykendall Andrew T.,
Talati Chetasi,
Padron Eric,
Sweet Kendra,
Lancet Jeffrey E.,
List Alan F.,
Sallman David,
Komrokji Rami S.
Publication year - 2019
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.25625
Subject(s) - myelofibrosis , essential thrombocythemia , calreticulin , thrombopoietin receptor , mutation , cancer research , medicine , janus kinase 2 , myeloid , myeloid leukemia , polycythemia vera , biology , haematopoiesis , gene , genetics , thrombopoietin , stem cell , bone marrow , receptor , endoplasmic reticulum
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