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. 2020 Aug 20;11:847. doi: 10.3389/fgene.2020.00847

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Copyright © 2020 Liang, Shao, Deng, Wang and Kang.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Prognosis and gene alteration of WIPI3 in HCC. (A) The OncoPrint schematic showed that gene alteration of WIPI3 occurred in 27 (7.16%) of all 377 sequenced cases, including truncating mutation in 2 cases (0.53%), amplification in 24 cases (6.37%), and deep deletion in 1 case (0.27); Kaplan–Meier (KM) survival curves for overall survival in normal and overall LIHC patients from the UALCAN database (B), the Gene Expression Profiling Interactive Analysis (GEPIA) database (C), and between gene alteration of WIPI3 (D).