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Article

Lack of SF3B1 R625 mutations in cutaneous melanoma.

Diagnostic pathology - 21 May 2013

Schilling Bastian, Bielefeld Nicola, Sucker Antje, Hillen Uwe, Zimmer Lisa, Schadendorf Dirk, Zeschnigk Michael, Griewank Klaus G

Abstract excerpt

BACKGROUND: Melanoma is a deadly disease affecting people worldwide. Genetic studies have identified different melanoma subtypes characterized by specific recurrently mutated genes and led to the successful clinical introduction of targeted therapies. Hotspot mutations in SF3B1 were recently reported in uveal melanoma. Our aim was to see if these mutations also occur in cutaneous melanoma. FINDINGS: We analyzed a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 23694694
DOI: 10.1186/1746-1596-8-87
PMCID: PMC3671181

Genes

BRAF
NRAS
KIT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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