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Phenotype and genotype analyses of 21 Chinese patients with Dent disease

Ruochen Che Yuwen Cai Wei Zhou Sanlong Zhao Songming Huang

Journal of Biomedical Research2025,Vol.39Issue(4):P.356-366,I0004-I0007,15.
Journal of Biomedical Research2025,Vol.39Issue(4):P.356-366,I0004-I0007,15.DOI:10.7555/JBR.38.20240183

Phenotype and genotype analyses of 21 Chinese patients with Dent disease

Ruochen Che 1Yuwen Cai 1Wei Zhou 2Sanlong Zhao 1Songming Huang3

作者信息

  • 1. Department of Nephrology,Children''s Hospital of Nanjing Medical University,Nanjing,Jiangsu 210029,China
  • 2. Nanjing Key Laboratory of Pediatrics,Children''s Hospital of Nanjing Medical University,Nanjing,Jiangsu 210029,China
  • 3. Department of Nephrology,Children''s Hospital of Nanjing Medical University,Nanjing,Jiangsu 210029,China Jiangsu Key Laboratory of Pediatrics,Nanjing Medical University,Nanjing,Jiangsu 211166,China
  • 折叠

摘要

关键词

Dent disease/CLCN5 gene/OCRL gene/low-molecular-weight proteinuria/children/X-chromosome inactivation

分类

医药卫生

引用本文复制引用

Ruochen Che,Yuwen Cai,Wei Zhou,Sanlong Zhao,Songming Huang..Phenotype and genotype analyses of 21 Chinese patients with Dent disease[J].Journal of Biomedical Research,2025,39(4):P.356-366,I0004-I0007,15.

基金项目

supported by the National Natural Science Foundation of China(Grant No.82200744) (Grant No.82200744)

the Nanjing Science and Technology Development Funding(Grant No.YKK22159). (Grant No.YKK22159)

Journal of Biomedical Research

1674-8301

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