Clinical Performance ofJAK2V617F Mutation Detection Assays in a Molecular Diagnostics Laboratory
Author:
Publisher
Oxford University Press (OUP)
Subject
General Medicine
Link
http://academic.oup.com/ajcp/article-pdf/132/5/713/5003643/ajcpath132-0713.pdf
Reference29 articles.
1. Myeloproliferative disorders
2. Table of contents
3. The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia
4. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
5. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
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2. CRISPR/Cas12a-Based Ultrasensitive and Rapid Detection of JAK2 V617F Somatic Mutation in Myeloproliferative Neoplasms;Biosensors;2021-07-24
3. Optimization of a Low-Cost, Sensitive PNA Clamping PCR Method for JAK2 V617F Variant Detection;The Journal of Applied Laboratory Medicine;2020-03-20
4. Clinical Implications of Quantitative JAK2 V617F Analysis using Droplet Digital PCR in Myeloproliferative Neoplasms;Annals of Laboratory Medicine;2018-03-28
5. Summary and Review of the Abstracts on Philadelphia-Negative Myeloproliferative Neoplasms Presented at Haematocon 2017;Indian Journal of Hematology and Blood Transfusion;2018-02-03
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