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Article

JAK2 V617F: a single mutation in the myeloproliferative group of disorders.

The Ulster medical journal - 1 May 2006

McLornan Donal, Percy Melanie, McMullin Mary Frances

Abstract excerpt

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Topics

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Share to DNA Mutational Analysis
Share to JAK2 gene
Share to Janus Kinase 2
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Myeloproliferative Disorders

Share to Protein-Tyrosine Kinases

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Source

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Identifiers

PMID: 16755940
PMCID: PMC1891745

Genes

JAK2

Variants

Provenance

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Update on the impact of the JAK2 mutation on signalling pathways in myeloproliferative disorders.Semantic proximity Read ↗

Genetic basis of MPN: Beyond JAK2-V617F.Semantic proximity Read ↗

[Myeloproliferative diseases caused by Jak2 gene mutation].Semantic proximity Read ↗

BCR/ABL-negative chronic myeloproliferative disorders: JAK2 mutation and beyond.Semantic proximity Read ↗

JAK2 V617F in myeloid disorders: what do we know now, and where are we headed?Semantic proximity Read ↗

JAK2 mutations other than V617F: a novel mutation and mini review.Semantic proximity Read ↗

The JAK2(V617F) tyrosine kinase mutation in myeloproliferative disorders: Summary of published literature and a perspective.Semantic proximity Read ↗

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