中文
|
English
Home
|
Help
|
Contact
Return
CUBN mutation, a genetic cause of persistent proteinuria in children
10.3339/ckd.24.019
Author:
Jin-Soon SUH
1
Author Information
1. Department of Pediatrics, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea
Publication Type:
4
From:
Childhood Kidney Diseases 2024;28(3):87-89
Country
Republic of Korea
Language:
English