Correlation of mutation status and morphological changes in essential thrombocythaemia and myelofibrosis

Pathology. 2018 Oct;50(6):671-674. doi: 10.1016/j.pathol.2018.02.005. Epub 2018 Aug 7.

Authors

Chong Chyn Chua¹, Amanda Omerod², Joel Wight³, Surender Juneja², Daniela Zantomio⁴

Affiliations

¹ Department of Laboratory Haematology, Austin Pathology, Vic, Australia. Electronic address: cchyn.chua@gmail.com.
² Department of Laboratory Haematology, Royal Melbourne Hospital, Vic, Australia.
³ Clinical Haematology, Austin Health, Vic, Australia.
⁴ Department of Laboratory Haematology, Austin Pathology, Vic, Australia; Clinical Haematology, Austin Health, Vic, Australia.

PMID: 30097170
DOI: 10.1016/j.pathol.2018.02.005

No abstract available

Publication types

Letter

MeSH terms

Adult
Aged
Aged, 80 and over
Calreticulin / genetics
DNA Mutational Analysis
Female
Humans
Janus Kinase 2 / genetics
Male
Middle Aged
Mutation
Primary Myelofibrosis / genetics*
Receptors, Thrombopoietin / genetics
Retrospective Studies
Thrombocythemia, Essential / genetics*
Young Adult

Substances

CALR protein, human
Calreticulin
Receptors, Thrombopoietin
MPL protein, human
JAK2 protein, human
Janus Kinase 2