A novel variant in the G-protein receptor kinase (GRK1) causes Oguchi syndrome, type II, in an Egyptian family.
- DOI
- 10.1080/13816810.2025.2612272
- Published
- 2026 Jun
- Container
- Ophthalmic genetics
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1080/13816810.2025.2612272,
title = {A novel variant in the G-protein receptor kinase (GRK1) causes Oguchi syndrome, type II, in an Egyptian family.},
author = {Fathy N and Elbagoury NM and Abdel-Hamid MS and ElKitkat RS and Shehab AA},
year = {2026},
journal = {Ophthalmic genetics},
doi = {10.1080/13816810.2025.2612272},
url = {https://doi.org/10.1080/13816810.2025.2612272}
}RIS
TY - JOUR TI - A novel variant in the G-protein receptor kinase (GRK1) causes Oguchi syndrome, type II, in an Egyptian family. AU - Fathy N AU - Elbagoury NM AU - Abdel-Hamid MS AU - ElKitkat RS AU - Shehab AA PY - 2026 JO - Ophthalmic genetics DO - 10.1080/13816810.2025.2612272 UR - https://doi.org/10.1080/13816810.2025.2612272 ER -
APA
N, F., NM, E., MS, A., RS, E., & AA, S. (2026). A novel variant in the G-protein receptor kinase (GRK1) causes Oguchi syndrome, type II, in an Egyptian family.. Ophthalmic genetics. https://doi.org/10.1080/13816810.2025.2612272
Source records
- pubmed · retrieved 2026-09-26T09:06:30.528Z