Case Report: Pediatric CNS-isolated hemophagocytic lymphohistiocytosis secondary to uniparental disomy of PRF1 mutation.
- DOI
- 10.3389/fgene.2025.1528844
- Published
- 2025
- Container
- Frontiers in genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3389/fgene.2025.1528844,
title = {Case Report: Pediatric CNS-isolated hemophagocytic lymphohistiocytosis secondary to uniparental disomy of PRF1 mutation.},
author = {Xue J and Song Z and Zhao H and Yang C and Li F and Yi Z and Liu K and Zhang Y},
year = {2025},
journal = {Frontiers in genetics},
doi = {10.3389/fgene.2025.1528844},
url = {https://doi.org/10.3389/fgene.2025.1528844}
}RIS
TY - JOUR TI - Case Report: Pediatric CNS-isolated hemophagocytic lymphohistiocytosis secondary to uniparental disomy of PRF1 mutation. AU - Xue J AU - Song Z AU - Zhao H AU - Yang C AU - Li F AU - Yi Z AU - Liu K AU - Zhang Y PY - 2025 JO - Frontiers in genetics DO - 10.3389/fgene.2025.1528844 UR - https://doi.org/10.3389/fgene.2025.1528844 ER -
APA
J, X., Z, S., H, Z., C, Y., F, L., Z, Y., K, L., & Y, Z. (2025). Case Report: Pediatric CNS-isolated hemophagocytic lymphohistiocytosis secondary to uniparental disomy of PRF1 mutation.. Frontiers in genetics. https://doi.org/10.3389/fgene.2025.1528844
Source records
- pubmed · retrieved 2026-09-26T03:21:01.988Z