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CUBN mutation, a genetic cause of persistent proteinuria in children

  • Jin-Soon Suh (Department of Pediatrics, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea)
  • Received : 2024.10.01
  • Accepted : 2024.10.15
  • Published : 2024.10.31

Abstract

Keywords

References

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  2. Boger CA, Chen MH, Tin A, Olden M, Kottgen A, de Boer IH, et al. CUBN is a gene locus for albuminuria. J Am Soc Nephrol 2011;22:555-70.
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