Clinical acceleration of JAK2 p.V617F driven myeloproliferative disease due to a new uncommon homozygous MPL p.Y591D mutation

Authors :: Andrew C. Perkins
Jeremy Ong
Helen Mitchell
Sue Morgan
Jane I. Lin
Source :: Haematologica
Publication Year :: 2020
Publisher :: Ferrata Storti Foundation (Haematologica), 2020.

Subjects :: Myeloproliferative Disorders
business.industry
Myeloproliferative disease
Acceleration (differential geometry)
Hematology
Janus Kinase 2
Text mining
JAK2 p.V617F
Mutation
Mutation (genetic algorithm)
Cancer research
Humans
Medicine
Online Only Articles
business
Receptors, Thrombopoietin

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