Primary hypertrophic osteoarthropathy complicated with myelofibrosis and compound heterozygous SLCO2A1 mutations: a case report and review of literature
- DOI
- 10.3389/fonc.2026.1772374
- Published
- 2026-06-30
- Container
- Frontiers in Oncology
- Publisher
- Frontiers Media SA
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3389/fonc.2026.1772374,
title = {Primary hypertrophic osteoarthropathy complicated with myelofibrosis and compound heterozygous SLCO2A1 mutations: a case report and review of literature},
author = {Qirui Xu and Qian Li and Jin Lu and Liru Wang},
year = {2026},
journal = {Frontiers in Oncology},
doi = {10.3389/fonc.2026.1772374},
url = {https://doi.org/10.3389/fonc.2026.1772374}
}RIS
TY - JOUR TI - Primary hypertrophic osteoarthropathy complicated with myelofibrosis and compound heterozygous SLCO2A1 mutations: a case report and review of literature AU - Qirui Xu AU - Qian Li AU - Jin Lu AU - Liru Wang PY - 2026 JO - Frontiers in Oncology DO - 10.3389/fonc.2026.1772374 UR - https://doi.org/10.3389/fonc.2026.1772374 ER -
APA
Xu, Q., Li, Q., Lu, J., & Wang, L. (2026). Primary hypertrophic osteoarthropathy complicated with myelofibrosis and compound heterozygous SLCO2A1 mutations: a case report and review of literature. Frontiers in Oncology. https://doi.org/10.3389/fonc.2026.1772374
Source records
- crossref · retrieved 2026-09-26T10:06:26.101Z