Unveiling long-standing low-molecular-weight proteinuria: A proximal tubular mitochondrial enzyme impairment caused by EHHADH mutation.
- DOI
- 10.1007/s00467-025-07020-9
- Published
- 2026 Mar
- Container
- Pediatric nephrology (Berlin, Germany)
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1007/s00467-025-07020-9,
title = {Unveiling long-standing low-molecular-weight proteinuria: A proximal tubular mitochondrial enzyme impairment caused by EHHADH mutation.},
author = {Tanaka H and Imasawa T and Tsugawa K and Inoki Y and Endo M and Nozu K},
year = {2026},
journal = {Pediatric nephrology (Berlin, Germany)},
doi = {10.1007/s00467-025-07020-9},
url = {https://doi.org/10.1007/s00467-025-07020-9}
}RIS
TY - JOUR TI - Unveiling long-standing low-molecular-weight proteinuria: A proximal tubular mitochondrial enzyme impairment caused by EHHADH mutation. AU - Tanaka H AU - Imasawa T AU - Tsugawa K AU - Inoki Y AU - Endo M AU - Nozu K PY - 2026 JO - Pediatric nephrology (Berlin, Germany) DO - 10.1007/s00467-025-07020-9 UR - https://doi.org/10.1007/s00467-025-07020-9 ER -
APA
H, T., T, I., K, T., Y, I., M, E., & K, N. (2026). Unveiling long-standing low-molecular-weight proteinuria: A proximal tubular mitochondrial enzyme impairment caused by EHHADH mutation.. Pediatric nephrology (Berlin, Germany). https://doi.org/10.1007/s00467-025-07020-9
Source records
- pubmed · retrieved 2026-09-27T08:50:45.783Z