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Article

Polycythemia vera and the Jak2(V617F) mutation in a case of hereditary spherocytosis.

The American journal of the medical sciences - 1 Oct 2013

Fleischman Roger A

Abstract excerpt

The identification of Jak2(V617F) mutations in more than 90% of patients with polycythemia vera (PV) has greatly improved the diagnostic accuracy for this uncommon myeloproliferative disorder. Although previous cases of presumptive PV in patients with hereditary spherocytosis (HS) have been descr...

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Source

Identifiers

PMID: 23588264
DOI: 10.1097/MAJ.0b013e31828c9df6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23588264-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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