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The JAK2 V617F mutation is not a cause of central retinal vein occlusion.
Primary tabs
| Document type | Article de périodique (Journal article) – Letter, Research Support, Non-U.S. Gov't |
|---|---|
| Access type | Accès restreint |
| Publication date | 2008 |
| Journal information | "Thrombosis and haemostasis" - Vol. 100, no. 3, p. 515-6 (2008) |
| Peer reviewed | yes |
| issn | 0340-6245 |
| Publication status | Publié |
| Affiliations |
UCL
- MD/MINT - Département de médecine interne UCL - MD/BICL - Département de biochimie et de biologie cellulaire UCL - (SLuc) Centre de malformations vasculaires congénitales UCL - (SLuc) Service d'hématologie UCL - (SLuc) Centre de génétique médicale UCL UCL - (SLuc) Centre de l'allergie |
| MESH Subject | Adult ; Aged ; Aged, 80 and over ; Alleles ; Female ; Humans ; Janus Kinase 2 - genetics ; Male ; Middle Aged ; Mutation ; Point Mutation ; Retinal Vein - pathology ; Retinal Vein Occlusion - genetics ; Risk Factors ; Thrombosis |
| Links |
| Bibliographic reference | Hermans, Cédric ; Lambert, Catherine ; Slachmuylder, Véronique ; Gala, Jean-Luc ; Detrait, Marie. The JAK2 V617F mutation is not a cause of central retinal vein occlusion.. In: Thrombosis and haemostasis, Vol. 100, no. 3, p. 515-6 (2008) |
|---|---|
| Permanent URL | http://hdl.handle.net/2078.1/29232 |