Detection of mutations in <i><scp>JAK</scp>2</i> exons 12–15 by Sanger sequencing

Abstract

JAK2 p.V617F was the most prevalent mutation detected among patients in this study. Non-p.V617F JAK2 mutations were identified in exons 12 and 13 corresponding to recently reported mutations, except for the novel p.I540_N542delinsM.