FSGS in Chinese twins with a de novo PAX2 mutation: a case report and review of the literature

J Nephrol. 2021 Dec;34(6):2155-2158. doi: 10.1007/s40620-021-01055-5. Epub 2021 May 4.
No abstract available

Publication types

  • Case Reports
  • Review

MeSH terms

  • China
  • Genetic Predisposition to Disease
  • Glomerulosclerosis, Focal Segmental*
  • Humans
  • Mutation
  • PAX2 Transcription Factor / genetics
  • Twins / genetics
  • Vesico-Ureteral Reflux*

Substances

  • PAX2 Transcription Factor
  • PAX2 protein, human