Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases by Rui Liang, Xuelan Chen, Ying Zhang, Chak-Fun Law, Sijie Yu, Jia Jiao, Qin Yang, Daoqi Wu, Gaofu Zhang, Han Chen, Mo Wang, Haiping Yang, Anshuo Wang

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Corrigendum: Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases by Rui Liang, Xuelan Chen, Ying Zhang, Chak-Fun Law, Sijie Yu, Jia Jiao, Qin Yang, Daoqi Wu, Gaofu Zhang, Han Chen, Mo Wang, Haiping Yang, Anshuo Wang

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Cell-type-specific molecular characterization of cells from circulation and kidney in IgA nephropathy with nephrotic syndrome by Qilin Chen, Qilin Chen, Qilin Chen, Huimin Jiang, Huimin Jiang, Huimin Jiang, Rong Ding, Jinjie Zhong, Jinjie Zhong, Jinjie Zhong, Longfei Li, Junli Wan, Junli Wan, Xiaoqian Feng, Xiaoqian Feng, Xiaoqian Feng, Liping Peng, Liping Peng, Liping Peng, Xia Yang, Xia Yang, Xia Yang, Han Chen, Han Chen, Anshuo Wang, Anshuo Wang, Jia Jiao, Jia Jiao, Qin Yang, Qin Yang, Xuelan Chen, Xuelan Chen, Xiaoqin Li, Xiaoqin Li, Lin Shi, Lin Shi, Gaofu Zhang, Gaofu Zhang, Mo Wang, Mo Wang, Haiping Yang, Haiping Yang, Qiu Li, Qiu Li, Qiu Li

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Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome by Jia Jiao, Li Wang, Fenfen Ni, Mo Wang, Shipin Feng, Xiaojie Gao, Han Chan, Xueying Yang, Hao Lee, Huan Chi, Xuelan Chen, Daoqi Wu, Gaofu Zhang, Baohui Yang, Anshuo Wang, Qin Yang, Junli Wan, Sijie Yu, Xiaoqin Li, Mei Wang, Xiaofeng Chen, Xianying Mai, Xiongzhong Ruan, Haiping Yang, Qiu Li

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