Volume 20 Issue 11
Nov.  2022
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doi: 10.16766/j.cnki.issn.1674-4152.002753
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 BK20210097

  • Received Date: 2021-10-15
    Available Online: 2022-12-30
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    FANG S H, DENG F, XU D L, et al. Clinical features and genetic variation analysis of 10 children with nephronephrhoea tuberculosis[J]. Anhui Medical Journal, 2021, 42(5): 498-501. https://www.cnki.com.cn/Article/CJFDTOTAL-AHYX202105008.htm
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    WANG D, TONG G X, DONG R, et al. Clinical and genetic analysis of a patient with rare nephronophthisis[J]. Chinese Journal of Medical Genetics, 2020, 37(7): 743-746. doi: 10.3760/cma.j.issn.1003-9406.2020.07.010
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    李国民, 刘海梅, 陈径, 等. NPHP3基因突变致婴幼儿期进展为终末期肾病的肾单位肾痨2例并文献复习[J]. 中国循证儿科杂志, 2017, 12(5): 362-367. doi: 10.3969/j.issn.1673-5501.2017.05.009

    LI G M, LIU H D, CHEN J, et al. Progression to end-stage renal disease during infancy and early child in two children with juvenile nephronophthisis caused by NPHP3 gene mutation and literature review[J]. Chinese Journal of Evidence-Based Pediatrics, 2017, 12(5): 362-367. doi: 10.3969/j.issn.1673-5501.2017.05.009
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    XU X X, SUN Z Y, DENG F, et al. Progressing of Nephronophthisis with different NPHP gene variations to end-stage renal disease in 3 cases[J]. Journal of Clinical Pediatrics, 2021, 39(6): 433-436. doi: 10.3969/j.issn.1000-3606.2021.06.008
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    李弢, 徐云云, 陈卫萍, 等. 青少年型肾单位肾痨1例及文献复习[J]. 微循环学杂志, 2019, 29(1): 96-98. doi: 10.3969/j.issn.1005-1740.2019.01.022

    LI T, XU Y Y, CHEN W P, et al. Juvenile nephrotic tuberculosis: A case report and literature review[J]. Chinese Journal of Microcirculation, 2019, 29(1): 96-98. doi: 10.3969/j.issn.1005-1740.2019.01.022
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    YU H M, SHEN Q. Progress in genetics of NPHP related signaling pathway[J]. International Journal of Pediatrics, 2018, 45(1): 1-4. doi: 10.3760/cma.j.issn.1673-4408.2018.01.001
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    简珊, 魏骐骄, 刘雨桐, 等. 1例肾单位肾痨12型的临床特点及TTC21B基因型研究[J]. 中国当代儿科杂志, 2019, 21(6): 580-584. https://www.cnki.com.cn/Article/CJFDTOTAL-DDKZ201906018.htm

    JIAN S, WEI Q J, LIU Y T, et al. Clinical features and TTC21B genotype of a child with nephronophthisis type 12[J]. Chinese Journal of Contemporary Pediatrics, 2019, 21(6): 580-584. https://www.cnki.com.cn/Article/CJFDTOTAL-DDKZ201906018.htm
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    杨静. 肾单位肾痨临床特点及基因突变分析[D]. 武汉: 华中科技大学, 2019.

    YANG J. Clinical characteristics and gene mutation analysis of nephronophthisis[D]. Wuhan: Huazhong University of Science and Technology, 2019.
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