The First Case Series of Malattia Leventinese/Doyne Honeycomb Retinal Dystrophy in Türkiye Identified with EFEMP1 Gene Mutation.
- DOI
- 10.4274/tjo.galenos.2026.22892
- Published
- 2026 Aug 26
- Container
- Turkish journal of ophthalmology
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.4274/tjo.galenos.2026.22892,
title = {The First Case Series of Malattia Leventinese/Doyne Honeycomb Retinal Dystrophy in Türkiye Identified with EFEMP1 Gene Mutation.},
author = {İşbilir A and Güzel A and Kocabey M and Çağlayan AO and Kartı Ö and Ayhan Z and Saatci AO},
year = {2026},
journal = {Turkish journal of ophthalmology},
doi = {10.4274/tjo.galenos.2026.22892},
url = {https://doi.org/10.4274/tjo.galenos.2026.22892}
}RIS
TY - JOUR TI - The First Case Series of Malattia Leventinese/Doyne Honeycomb Retinal Dystrophy in Türkiye Identified with EFEMP1 Gene Mutation. AU - İşbilir A AU - Güzel A AU - Kocabey M AU - Çağlayan AO AU - Kartı Ö AU - Ayhan Z AU - Saatci AO PY - 2026 JO - Turkish journal of ophthalmology DO - 10.4274/tjo.galenos.2026.22892 UR - https://doi.org/10.4274/tjo.galenos.2026.22892 ER -
APA
A, İ., A, G., M, K., AO, Ç., Ö, K., Z, A., & AO, S. (2026). The First Case Series of Malattia Leventinese/Doyne Honeycomb Retinal Dystrophy in Türkiye Identified with EFEMP1 Gene Mutation.. Turkish journal of ophthalmology. https://doi.org/10.4274/tjo.galenos.2026.22892
Source records
- pubmed · retrieved 2026-09-26T07:34:54.548Z