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JAK2V617F mutation can occur exclusively in the erythroid lineage and be absent in granulocytes and progenitor cells in classic myeloproliferative disorders

✍ Scribed by Barbara K. Zehentner; Michael R. Loken; Denise A. Wells


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
338 KB
Volume
81
Category
Article
ISSN
0361-8609

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