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. 2022 Jan 31;8:810940. doi: 10.3389/fmed.2021.810940

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Copyright © 2022 Li, Zhu, Shi, Xu, Lv and Zhang.

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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Verification of WT1 and NPHS1 variants by Sanger sequencing. (A) The c.1397C>T; p.Ser466Phe mutation was verified in seven family members (III-6, IV-5, IV-7, IV-8, V-1, V-6, V-7, and VI-1). (B) The c.1433-10G>A mutation was verified in three family members (IV-8, V-6, and V-7). (C) The c.3478C>T; p.Arg1160Ter mutation was verified in five family members (III-6, III-7, IV-5, V-3, and VI-2).