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A JAK2 mutation in myeloproliferative disorders: pathogenesis and therapeutic and scientific prospects

✍ Scribed by Chloé James; Valérie Ugo; Nicole Casadevall; Stefan N. Constantinescu; William Vainchenker

Book ID: 116757980
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 362 KB
Volume: 11
Category: Article
ISSN: 1471-4914
DOI: 10.1016/j.molmed.2005.10.003

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## background Polycythemia vera, essential thrombocythemia, and idiopathic myelofibrosis are clonal myeloproliferative disorders arising from a multipotent progenitor. The loss of heterozygosity (LOH) on the short arm of chromosome 9 (9pLOH) in myeloproliferative disorders suggests that 9p harbors