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The mutant JAK2V617F allele burden in children with essential thrombocythemia

✍ Scribed by Luciana Teofili; Tonia Cenci; Maurizio Martini; Sara Capodimonti; Lorenza Torti; Fiorina Giona; Angela Amendola; Maria Luigia Randi; Maria Caterina Putti; Margherita Scapin; Giuseppe Leone; Luigi Maria Larocca


Book ID
108676197
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
97 KB
Volume
145
Category
Article
ISSN
0007-1048

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Clinical correlates of JAK2V617F allele
✍ Jaya Kittur; Ryan A. Knudson; Terra L. Lasho; Christy M. Finke; Naseema Gangat; πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 198 KB

## Abstract ## BACKGROUND. __JAK2__V617F occurs in approximately 50% of patients with essential thrombocythemia (ET). Qualitative studies of mutation analysis have previously reported an association between __JAK2__V617F and advanced age, higher hemoglobin level, higher leukocyte count, and lower