Prevalence of the JAK2 V617F mutation associated with splanchnic vein thrombosis. A 10-year retrospective study
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Veröffentlicht in: | Thrombosis and haemostasis 2009-04, Vol.101 (4), p.787-789 |
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container_title | Thrombosis and haemostasis |
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creator | Tondeur, Sylvie Boutruche, Sandrine Biron-Andréani, Christine Schved, Jean-François |
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doi_str_mv | 10.1160/TH08-07-0451 |
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language | eng |
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source | MEDLINE; Thieme Connect Journals |
subjects | Adolescent Adult Aged Budd-Chiari Syndrome - blood Budd-Chiari Syndrome - enzymology Budd-Chiari Syndrome - genetics Female Gene Frequency Genetic Predisposition to Disease Humans Janus Kinase 2 - genetics Letters to the Editor Male Middle Aged Mutation Myeloproliferative Disorders - blood Myeloproliferative Disorders - diagnosis Myeloproliferative Disorders - enzymology Myeloproliferative Disorders - genetics Polymorphism, Single Nucleotide Portal Vein Retrospective Studies Risk Assessment Risk Factors Time Factors Venous Thrombosis - blood Venous Thrombosis - enzymology Venous Thrombosis - genetics Young Adult |
title | Prevalence of the JAK2 V617F mutation associated with splanchnic vein thrombosis. A 10-year retrospective study |
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