Biochemical testing and pathology reveal rare cause of pediatric acute liver failure: Hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome
- DOI
- 10.1002/jpr3.70206
- Published
- 2026-07-27
- Container
- JPGN Reports
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/jpr3.70206,
title = {Biochemical testing and pathology reveal rare cause of pediatric acute liver failure: Hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome},
author = {Tierra L. Mosher and Kathryn S. Czepiel and Matthew B. Neu and Andrea Carolina Cortes Fernandez and L. Walden Browne and Annie D. Niehaus and Roberto Gugig},
year = {2026},
journal = {JPGN Reports},
doi = {10.1002/jpr3.70206},
url = {https://doi.org/10.1002/jpr3.70206}
}RIS
TY - JOUR TI - Biochemical testing and pathology reveal rare cause of pediatric acute liver failure: Hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome AU - Tierra L. Mosher AU - Kathryn S. Czepiel AU - Matthew B. Neu AU - Andrea Carolina Cortes Fernandez AU - L. Walden Browne AU - Annie D. Niehaus AU - Roberto Gugig PY - 2026 JO - JPGN Reports DO - 10.1002/jpr3.70206 UR - https://doi.org/10.1002/jpr3.70206 ER -
APA
Mosher, T. L., Czepiel, K. S., Neu, M. B., Fernandez, A. C. C., Browne, L. W., Niehaus, A. D., & Gugig, R. (2026). Biochemical testing and pathology reveal rare cause of pediatric acute liver failure: Hyperornithinemia‐hyperammonemia‐homocitrullinuria syndrome. JPGN Reports. https://doi.org/10.1002/jpr3.70206
Source records
- crossref · retrieved 2026-09-25T15:17:21.595Z