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SRSF2 Mutations in Uveal Melanoma: A Preference for In-Frame Deletions?
Background: Uveal melanoma (UM) is the most common primary ocular malignancy in adults in the Western world. UM with a mutation in SF3B1, a spliceosome gene, is characterized by three or more structural changes of chromosome 1, 6, 8, 9, or 11. Also UM without a mutation in SF3B1 harbors similar chro...
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| Publicado no: | Cancers (Basel) |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6721539/ https://ncbi.nlm.nih.gov/pubmed/31426461 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cancers11081200 |
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