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The V617F mutation of JAK2 is very uncommon in patients with thrombosis.
- Source :
-
Haematologica [Haematologica] 2007 Feb; Vol. 92 (2), pp. 285-6. - Publication Year :
- 2007
-
Abstract
- Given that many cases of thrombosis do not have a clear cause, a myeloproliferative disease could be involved. We investigated the V617F mutation of the JAK2 gene in 295 patients with thrombosis. Only one case was positive. Therefore, the study of this mutation is not necessary in all patients with idiopathic thrombosis.
- Subjects :
- Aged
Cohort Studies
Female
Hemoglobins metabolism
Humans
Male
Middle Aged
Polycythemia Vera complications
Polycythemia Vera genetics
Thrombocythemia, Essential complications
Thrombocythemia, Essential genetics
Janus Kinase 2 blood
Janus Kinase 2 genetics
Mutation
Thrombosis blood
Thrombosis genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1592-8721
- Volume :
- 92
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Haematologica
- Publication Type :
- Editorial & Opinion
- Accession number :
- 17296594
- Full Text :
- https://doi.org/10.3324/haematol.10358