Rare genetic variants in leber hereditary optic neuropathy: molecular mechanisms, diagnosis, and emerging therapies.
- DOI
- 10.1007/s10633-026-10166-y
- Published
- 2026 Nov 9
- Container
- Documenta ophthalmologica. Advances in ophthalmology
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1007/s10633-026-10166-y,
title = {Rare genetic variants in leber hereditary optic neuropathy: molecular mechanisms, diagnosis, and emerging therapies.},
author = {Chlebowska G and Michalak K and Gancek E and Lis M and Drzazga M and Lyp-Broszko A and Klaudel T and Strojek M and Pławszewski R},
year = {2026},
journal = {Documenta ophthalmologica. Advances in ophthalmology},
doi = {10.1007/s10633-026-10166-y},
url = {https://doi.org/10.1007/s10633-026-10166-y}
}RIS
TY - JOUR TI - Rare genetic variants in leber hereditary optic neuropathy: molecular mechanisms, diagnosis, and emerging therapies. AU - Chlebowska G AU - Michalak K AU - Gancek E AU - Lis M AU - Drzazga M AU - Lyp-Broszko A AU - Klaudel T AU - Strojek M AU - Pławszewski R PY - 2026 JO - Documenta ophthalmologica. Advances in ophthalmology DO - 10.1007/s10633-026-10166-y UR - https://doi.org/10.1007/s10633-026-10166-y ER -
APA
G, C., K, M., E, G., M, L., M, D., A, L., T, K., M, S., & R, P. (2026). Rare genetic variants in leber hereditary optic neuropathy: molecular mechanisms, diagnosis, and emerging therapies.. Documenta ophthalmologica. Advances in ophthalmology. https://doi.org/10.1007/s10633-026-10166-y
Source records
- pubmed · retrieved 2026-11-10T11:21:18.242Z