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Besides, we additionally received a list of genes with bad prognosis in GBM. Finally, we derived a risk-gene signature with three selected m6A RNA methylation regulators, which allowed us to give the in-depth research and dichotomized the OS of patients with GBM into large- and low-risk subgroups. Particularly, this risk-gene trademark could possibly be made use of as independent prognostic markers and accurate clinicopathological parameter predictors. In conclusion, m6A RNA meth
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