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Article

Absence of PPP2R1A mutations in Wilms tumor.

Oncogene - 12 Apr 2001

Ruteshouser E C, Ashworth L K, Huff V

Abstract excerpt

Evidence from genetic linkage analysis indicates that a gene located at 19q13.4, FWT2, is responsible for predisposition to Wilms tumor in many Wilms tumor families. This region has also been implicated in the etiology of sporadic Wilms tumor through loss of heterozygosity analyses. The PPP2R1A gene, encoding the alpha isoform of the heterotrimeric serine/threonine protein phosphatase 2A (PP2A), is located within...

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Identifiers

PMID: 11360189
DOI: 10.1038/sj.onc.1204301

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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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Semantic proximity does not establish scientific evidence.

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Absence of PPP2R1A mutations in Wilms tumor.PMID 11360189Read ↗

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