JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia.
In: Journal of Clinical Pathology, Jg. 65 (2012-10-01), Heft 10, S. 953-955
academicJournal
Zugriff:
The article explains the connection on JAK2V617F mutation and allele burden in determining clinical and morphological subtypes among essential thrombocythaemia (ET) patients. A study was performed on 103 patients at the S. Giovanni Hospital and University of Turin from 2006 to 2010, were various diseases linked to mutation were assessed like splenomegaly and arterial thrombosis. Results showed that ET patients with JAK2V617F mutation were shown with a photocythaemia vera-like phenotype.
| Titel: |
JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia.
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| Autor/in / Beteiligte Person: | Pich, Achille ; Riera, Ludovica ; Beggiato, Eloise ; Nicolino, Barbara ; Godio, Laura ; Campisi, Paola ; Sismondi, Francesca ; di Celle, Paola Francia |
| Zeitschrift: | Journal of Clinical Pathology, Jg. 65 (2012-10-01), Heft 10, S. 953-955 |
| Veröffentlichung: | 2012 |
| Medientyp: | academicJournal |
| ISSN: | 0021-9746 (print) |
| DOI: | 10.1136/jclinpath-2012-200804 |
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