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The JAK2V617F tyrosine kinase mutation identifies clinically latent myeloproliferative disorders in patients presenting with hepatic or portal vein thrombosis

✍ Scribed by C. GOULDING; B. UTTENTHAL; L. FORONI; V. DUKE; A. TRAORE; P. KOTTARIDIS; A. V. HOFFBRAND; D. PATCH; C. MCNAMARA

Book ID: 111415055
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 66 KB
Volume: 30
Category: Article
ISSN: 1751-5521
DOI: 10.1111/j.1751-553x.2007.00973.x

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