Hasil Pencarian - Linxia Deng
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CUBN gene mutations may cause focal segmental glomerulosclerosis (FSGS) in children oleh Jing Yang, Yongli Xu, Linxia Deng, Luowen Zhou, Liru Qiu, Yu Zhang, Jianhua Zhou
Diterbitkan 2022-01-01
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Novel pathogenic OCRL mutations and genotype–phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review oleh Yu Zhang, Linxia Deng, Xiaohong Chen, Yingjie Hu, Yaxian Chen, Kang Chen, Jianhua Zhou
Diterbitkan 2021-09-01
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