<i>JAK2</i> Mutations Are Rare and Diverse in Myelodysplastic Syndromes: Case Series and Review of the Literature.

Hematol Rep · 2023 · PMC9944460 · PMID 36810551

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indeterminate significanceno p-value reported

Interestingly, the inherited bone marrow failure molecular panel detected a heterozygous SAMD9 variant of indeterminate significance.

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