CUBN mutation, a genetic cause of persistent proteinuria in children.

Suh JS

DOI: 10.3339/ckd.24.019
Published: 2024 Oct
Container: Childhood kidney diseases
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3339/ckd.24.019,
  title = {CUBN mutation, a genetic cause of persistent proteinuria in children.},
  author = {Suh JS},
  year = {2024},
  journal = {Childhood kidney diseases},
  doi = {10.3339/ckd.24.019},
  url = {https://doi.org/10.3339/ckd.24.019}
}

RIS

TY  - JOUR
TI  - CUBN mutation, a genetic cause of persistent proteinuria in children.
AU  - Suh JS
PY  - 2024
JO  - Childhood kidney diseases
DO  - 10.3339/ckd.24.019
UR  - https://doi.org/10.3339/ckd.24.019
ER  -

APA

JS, S. (2024). CUBN mutation, a genetic cause of persistent proteinuria in children.. Childhood kidney diseases. https://doi.org/10.3339/ckd.24.019

Source records

pubmed · retrieved 2026-09-27T15:41:36.985Z