Crigler-Najjar syndrome type 2 complicating cholecystitis in a patient with UGT1A1 gene double homozygous mutations.

Zhang J, Chen R, Chen X, Chen Y, Chen Q, Lu S, Luo J, Zheng X, Chen M

DOI: 10.1007/s11684-025-1142-6
Published: 2025 Aug
Container: Frontiers of medicine
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1007/s11684-025-1142-6,
  title = {Crigler-Najjar syndrome type 2 complicating cholecystitis in a patient with UGT1A1 gene double homozygous mutations.},
  author = {Zhang J and Chen R and Chen X and Chen Y and Chen Q and Lu S and Luo J and Zheng X and Chen M},
  year = {2025},
  journal = {Frontiers of medicine},
  doi = {10.1007/s11684-025-1142-6},
  url = {https://doi.org/10.1007/s11684-025-1142-6}
}

RIS

TY  - JOUR
TI  - Crigler-Najjar syndrome type 2 complicating cholecystitis in a patient with UGT1A1 gene double homozygous mutations.
AU  - Zhang J
AU  - Chen R
AU  - Chen X
AU  - Chen Y
AU  - Chen Q
AU  - Lu S
AU  - Luo J
AU  - Zheng X
AU  - Chen M
PY  - 2025
JO  - Frontiers of medicine
DO  - 10.1007/s11684-025-1142-6
UR  - https://doi.org/10.1007/s11684-025-1142-6
ER  -

APA

J, Z., R, C., X, C., Y, C., Q, C., S, L., J, L., X, Z., & M, C. (2025). Crigler-Najjar syndrome type 2 complicating cholecystitis in a patient with UGT1A1 gene double homozygous mutations.. Frontiers of medicine. https://doi.org/10.1007/s11684-025-1142-6

Source records

pubmed · retrieved 2026-11-10T12:11:12.123Z