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Impact of JAK2V617F Mutational Status on Phenotypic Features in Essential Thrombocythemia and Primary Myelofibrosis

dc.contributor.authorNalcaci, Meliha
dc.contributor.authorDaglar-Aday, Aynur
dc.contributor.authorYilmaz, Ceylan
dc.contributor.authorSargin, Fatma Deniz
dc.contributor.authorYonal, Ipek
dc.contributor.authorAkadam-Teker, Basak
dc.contributor.authorYavuz, Akif
dc.date.accessioned2021-03-03T16:39:15Z
dc.date.available2021-03-03T16:39:15Z
dc.date.issued2016
dc.identifier.citationYonal I., Daglar-Aday A., Akadam-Teker B., Yilmaz C., Nalcaci M., Yavuz A., Sargin F. D. , "Impact of JAK2V617F Mutational Status on Phenotypic Features in Essential Thrombocythemia and Primary Myelofibrosis", TURKISH JOURNAL OF HEMATOLOGY, cilt.33, sa.2, ss.94-101, 2016
dc.identifier.issn1300-7777
dc.identifier.othervv_1032021
dc.identifier.otherav_455c1e0b-fa93-4cda-8e9b-f631dea8cbe3
dc.identifier.urihttp://hdl.handle.net/20.500.12627/50309
dc.identifier.urihttps://doi.org/10.4274/tjh.2014.0136
dc.description.abstractObjective: The JAK2V617F mutation is present in the majority of patients with essential thrombocythemia (ET) and primary myelofibrosis (PMF). The impact of this mutation on disease phenotype in ET and PMF is still a matter of discussion. This study aims to determine whether there are differences in clinical presentation and disease outcome between ET and PMF patients with and without the JAK2V617F mutation.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.subjectHEMATOLOJİ
dc.titleImpact of JAK2V617F Mutational Status on Phenotypic Features in Essential Thrombocythemia and Primary Myelofibrosis
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF HEMATOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume33
dc.identifier.issue2
dc.identifier.startpage94
dc.identifier.endpage101
dc.contributor.firstauthorID227445


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