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  • JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia

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JAK2V617F mutation and allele burden are associated with distinct clinical and morphological subtypes in patients with essential thrombocythaemia

https://doi.org/10.1136/jclinpath-2012-200804

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    Footnotes

    • Funding This work was supported by grants from the Italian Ministero dell'Università e Ricerca Scientifica e Tecnologica (MURST).

    • Competing interests None.

    • Ethics approval Ethics approval was provided by Ethics Committee of A.S.O San Giovanni Battista—A.S.O. C.T.O./C.R.F./ Maria Adelaide of Turin.

    • Provenance and peer review Not commissioned; externally peer reviewed.