The JAK2(V617F) tyrosine kinase mutation in blood donors with upper-limit haematocrit levels

It is not rare to observe in blood donors a level of haematocrit (Hct) above or close to the highest normal limit. In the case of blood donors the diagnosis and clinical evaluation of this alteration may be complicated by regular blood donations that can mask an underlying disease such as polycythae...

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Veröffentlicht in:	Blood transfusion = Trasfusione del sangue 2009-04, Vol.7 (2), p.111
Hauptverfasser:	Tagariello, Giuseppe, Di Gaetano, Rosanna, Sartori, Roberto, Zanotto, Daniela, Belvini, Donata, Radossi, Paolo, Risato, Renzo, Roveroni, Giovanni, Salviato, Roberta, Tassinari, Cristina, Toffano, Nunzio
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Blood Donors Chromosomes, Human, Pair 9 - genetics Diagnosis, Differential Female Genetic Testing Hematocrit Humans Incidence Italy - epidemiology Janus Kinase 2 - genetics Male Middle Aged Mutation Myeloproliferative Disorders - blood Myeloproliferative Disorders - diagnosis Myeloproliferative Disorders - epidemiology Myeloproliferative Disorders - genetics Phenotype Polycythemia Vera - blood Polycythemia Vera - diagnosis Polycythemia Vera - epidemiology Polycythemia Vera - genetics Prevalence Retrospective Studies
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