Case Report: Type II tyrosinemia caused by mutations at the c.843_844 inv p.(Trp282Gly) variant locus

Fei Tong, Meirong Peng, Lingzhang Meng, Jiajia Shen, Lin Huang, Weifang Huang, Weitong Huang, Jian Song

Open source

DOI: 10.3389/fgene.2026.1753440
Published: 2026-03-12
Container: Frontiers in Genetics
Publisher: Frontiers Media SA
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3389/fgene.2026.1753440,
  title = {Case Report: Type II tyrosinemia caused by mutations at the c.843\_844 inv p.(Trp282Gly) variant locus},
  author = {Fei Tong and Meirong Peng and Lingzhang Meng and Jiajia Shen and Lin Huang and Weifang Huang and Weitong Huang and Jian Song},
  year = {2026},
  journal = {Frontiers in Genetics},
  doi = {10.3389/fgene.2026.1753440},
  url = {https://doi.org/10.3389/fgene.2026.1753440}
}

RIS

TY  - JOUR
TI  - Case Report: Type II tyrosinemia caused by mutations at the c.843_844 inv p.(Trp282Gly) variant locus
AU  - Fei Tong
AU  - Meirong Peng
AU  - Lingzhang Meng
AU  - Jiajia Shen
AU  - Lin Huang
AU  - Weifang Huang
AU  - Weitong Huang
AU  - Jian Song
PY  - 2026
JO  - Frontiers in Genetics
DO  - 10.3389/fgene.2026.1753440
UR  - https://doi.org/10.3389/fgene.2026.1753440
ER  -

APA

Tong, F., Peng, M., Meng, L., Shen, J., Huang, L., Huang, W., Huang, W., & Song, J. (2026). Case Report: Type II tyrosinemia caused by mutations at the c.843_844 inv p.(Trp282Gly) variant locus. Frontiers in Genetics. https://doi.org/10.3389/fgene.2026.1753440

Source records

crossref · retrieved 2026-09-25T08:15:00.740Z