Associated Papers
Novel BEST1 Variant Characterization in a Large French Cohort in Light of Updated Bestrophin-1 Structure-Function Correlation.
Bitan J et al.
Investigative Ophthalmology & Visual Science, 2025
40891781 (PubMed )
Supplement: iovs-66-12-4_s009.xlsx › A._Variants_description
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy.
Karali M et al.
Scientific Reports, 2022
36460718 (PubMed )
Supplement: 41598_2022_24636_MOESM2_ESM.xlsx › Supplementary_Table_S1
Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study.
Low S et al.
Molecular Vision, 2011
A normal electro-oculography in a family affected by best disease with a novel spontaneous mutation of the BEST1 gene.
Testa F et al.
The British Journal of Ophthalmology, 2008
Normal electro-oculography in a young Omani male with genetically confirmed best disease complicated by choroidal neovascularization.
Al-Abri M et al.
Oman Journal of Ophthalmology, 0
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