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Prevalence of the frequency of JAK2 (V617F) mutation in different myeloproliferative disorders in Egyptian patients

Background and objectives: Detection of chromosomal abnormalities in myeloproliferative disorders is important for proper diagnosis of these disorders. This study has investigated the presence of JAK2 mutation (V617F) in Egyptian patients with myeloproliferative disorders referred to National Cancer...

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Publicat a:Int J Clin Exp Pathol
Autors principals: Ebid, Gamal T, Ghareeb, Mohamed, Salaheldin, Omina, Kamel, Mahmoud M
Format: Artigo
Idioma:Inglês
Publicat: e-Century Publishing Corporation 2015
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4637706/
https://ncbi.nlm.nih.gov/pubmed/26617890
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