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JAK2-V617F mutation in Moroccan patients with myeloproliferative disorders: Contribution, diagnosis and therapeutic prospects

✍ Scribed by A. Benmoussa; H. Dehbi; S. Fehri; A. Quessar; S. Nadifi


Book ID
115542142
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
177 KB
Volume
59
Category
Article
ISSN
0369-8114

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Correlations of JAK2–V617F mutation with
✍ Matthaios Speletas; Eirini Katodritou; Chrisoula Daiou; Eudokia Mandala; Emmanou πŸ“‚ Article πŸ“… 2007 πŸ› Elsevier Science 🌐 English βš– 212 KB

Recently, the acquired mutation JAK2-V617F has been described in the majority of patients with myeloproliferative disorders (MPDs). In this study we evaluated its clinical and laboratory correlates in 166 patients with MPDs. The mutation was detected by allele-specific PCR in 119 patients: 81.4% (35