Different CALR mutation subtypes in essential thrombocythemia and primary myelofibrosis patients without JAK2 mutation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Hematology
Link
http://link.springer.com/content/pdf/10.1007/s12254-020-00584-2.pdf
Reference32 articles.
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2. Campbell PJ, Green AR. The myeloproliferative disorders. N Engl J Med. 2006;355:2452–66. https://doi.org/10.1056/NEJMra063728.
3. Jeong JH, Lee HT, Seo JY, Seo YH, Kim KH, Kim MJ, et al. Screening PCR versus sanger sequencing: detection of CALR mutations in patients with thrombocytosis. Ann Lab Med. 2016;36:291–9. https://doi.org/10.3343/alm.2016.36.4.291.
4. Pikman Y, Lee BH, Mercher T, McDowell E, Ebert BL, Gozo M, et al. MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia. PLoS Med. 2006;3:e270. https://doi.org/10.1371/journal.pmed.0030270.
5. Pardanani AD, Levine RL, Lasho T, Pikman Y, Mesa RA, Wadleigh M, et al. MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients. Blood. 2006;108:3472–6. https://doi.org/10.1182/blood-2006-04-018879.
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