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Article

Mutation of FLT3 gene in acute myeloid leukemia with normal cytogenetics and its association with clinical and immunophenotypic features.

Medical oncology (Northwood, London, England) - 1 Jun 2011

Chauhan Pradeep S, Bhushan Bharat, Mishra Ashwani K, Singh Laishram C, Saluja Sumita, Verma Saurabh, Gupta Dipendra K, Mittal Vishakha, Chaudhry Sumita, Kapur Sujala

Abstract excerpt

Acute myeloid leukemia (AML) with normal karyotype represents a clinically and molecularly heterogeneous disease. Molecular markers with prognostic significance have been examined to improve risk profile characterization of this group. Activating mutations on FLT3 receptor are one of the most common genetic alterations reported. However, the prevalence and prognostic significance of FLT3 genetic alterations in...

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PMID: 20354824
DOI: 10.1007/s12032-010-9485-4

Genes

FLT3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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