JAK2 V617F mutation in combination of ASXL1, DNMT3, TET2, U2AF1 and RUNX1 variants is associated with severe clinical phenotypes in primary myelofibrosis.

GIN, GAN SHIAW SZE @ GAN GIN (2015) JAK2 V617F mutation in combination of ASXL1, DNMT3, TET2, U2AF1 and RUNX1 variants is associated with severe clinical phenotypes in primary myelofibrosis. hameatologica.

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Item Type: Other
Uncontrolled Keywords: JAK2 V617F mutation in combination of ASXL1, DNMT3, TET2, U2AF1 and RUNX1 variants is associated wi
Subjects: R Medicine
Depositing User: MR. ADNAN YAHYA
Date Deposited: 23 Dec 2015
Last Modified: 23 Dec 2015
URI: http://repository.um.edu.my/id/eprint/107755

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