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Deep sequencing of uveal melanoma identifies a recurrent mutation in PLCB4
Next generation sequencing of uveal melanoma (UM) samples has identified a number of recurrent oncogenic or loss-of-function mutations in key driver genes including: GNAQ, GNA11, EIF1AX, SF3B1 and BAP1. To search for additional driver mutations in this tumor type we carried out whole-genome or whole...
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Udgivet i: | Oncotarget |
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Main Authors: | , , , , , , , , , , , , , , , , , , |
Format: | Artigo |
Sprog: | Inglês |
Udgivet: |
Impact Journals LLC
2015
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Fag: | |
Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4826231/ https://ncbi.nlm.nih.gov/pubmed/26683228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.6614 |
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