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Article

A new DNA-based test for detection of nucleophosmin exon 12 mutations by capillary electrophoresis.

The Journal of molecular diagnostics : JMD - 1 May 2008

Szankasi Philippe, Jama Mohamed, Bahler David W

Abstract excerpt

Mutations in nucleophosmin (NPM1) exon 12 are thought to be the most common genetic event in acute myelogenous leukemia (AML) and to confer favorable clinical prognoses. In this report, we describe a simple molecular test for the detection of NPM1 exon 12 mutations in patients with AML using poly...

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Share to Electrophoresis, Capillary
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukemia, Myeloid, Acute

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Source

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Identifiers

PMID: 18403605
DOI: 10.2353/jmoldx.2008.070167
PMCID: PMC2329788

Genes

NPM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18403605-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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