Case Report: Clinical and genetic analysis of a Bietti crystalline dystrophy family with multisite crystalline deposits and a phenotype of macular hole combined with retinoschisis.
- DOI
- 10.3389/fmed.2025.1664126
- Published
- 2025
- Container
- Frontiers in medicine
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3389/fmed.2025.1664126,
title = {Case Report: Clinical and genetic analysis of a Bietti crystalline dystrophy family with multisite crystalline deposits and a phenotype of macular hole combined with retinoschisis.},
author = {Zheng CY and Chen H and Jiang YY and Lu H},
year = {2025},
journal = {Frontiers in medicine},
doi = {10.3389/fmed.2025.1664126},
url = {https://doi.org/10.3389/fmed.2025.1664126}
}RIS
TY - JOUR TI - Case Report: Clinical and genetic analysis of a Bietti crystalline dystrophy family with multisite crystalline deposits and a phenotype of macular hole combined with retinoschisis. AU - Zheng CY AU - Chen H AU - Jiang YY AU - Lu H PY - 2025 JO - Frontiers in medicine DO - 10.3389/fmed.2025.1664126 UR - https://doi.org/10.3389/fmed.2025.1664126 ER -
APA
CY, Z., H, C., YY, J., & H, L. (2025). Case Report: Clinical and genetic analysis of a Bietti crystalline dystrophy family with multisite crystalline deposits and a phenotype of macular hole combined with retinoschisis.. Frontiers in medicine. https://doi.org/10.3389/fmed.2025.1664126
Source records
- pubmed · retrieved 2026-09-25T08:16:42.517Z