Isolated benign persistent proteinuria with novel association of
cubilin gene
genetic testing
kidney
monogenic
persistent proteinuria
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Jun 2023
Jun 2023
Historique:
received:
02
03
2023
revised:
18
05
2023
accepted:
29
05
2023
medline:
14
6
2023
pubmed:
14
6
2023
entrez:
14
6
2023
Statut:
epublish
Résumé
We present two siblings with persistent proteinuria and normal kidney function, each carrying the same compound heterozygous variants in the
Identifiants
pubmed: 37312928
doi: 10.1002/ccr3.7502
pii: CCR37502
pmc: PMC10258721
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e7502Informations de copyright
© 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
QS, DC, and SP are full‐time employees at Natera Inc. with stocks or options to own stocks in the company. VS, RK, and MF declare no conflicts of interest.
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