Genotype–Phenotype Correlation in Dominant Optic Atrophy due to OPA1 c.3011T>C (p.Leu1004Pro): A Family-Based Case Series
- DOI
- 10.4103/joco.joco_4_26
- Published
- 2026-01
- Container
- Journal of Current Ophthalmology
- Publisher
- Ovid Technologies (Wolters Kluwer Health)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.4103/joco.joco_4_26,
title = {Genotype–Phenotype Correlation in Dominant Optic Atrophy due to OPA1 c.3011T\>C (p.Leu1004Pro): A Family-Based Case Series},
author = {Hasan Can Küçük and Nilüfer Koçak and Denizcan Özizmirliler and Suzan Doğruya and Ali Devebacak},
year = {2026},
journal = {Journal of Current Ophthalmology},
doi = {10.4103/joco.joco_4_26},
url = {https://doi.org/10.4103/joco.joco_4_26}
}RIS
TY - JOUR TI - Genotype–Phenotype Correlation in Dominant Optic Atrophy due to OPA1 c.3011T>C (p.Leu1004Pro): A Family-Based Case Series AU - Hasan Can Küçük AU - Nilüfer Koçak AU - Denizcan Özizmirliler AU - Suzan Doğruya AU - Ali Devebacak PY - 2026 JO - Journal of Current Ophthalmology DO - 10.4103/joco.joco_4_26 UR - https://doi.org/10.4103/joco.joco_4_26 ER -
APA
Küçük, H. C., Koçak, N., Özizmirliler, D., Doğruya, S., & Devebacak, A. (2026). Genotype–Phenotype Correlation in Dominant Optic Atrophy due to OPA1 c.3011T>C (p.Leu1004Pro): A Family-Based Case Series. Journal of Current Ophthalmology. https://doi.org/10.4103/joco.joco_4_26
Source records
- crossref · retrieved 2026-09-25T00:48:59.772Z