Associated Papers
The genetic landscape of inherited retinal dystrophies in Arabs.
Jaffal L et al.
Bmc Medical Genomics, 2023
37127645 (PubMed )
Supplement: 12920_2023_1518_MOESM2_ESM.xlsx › Sheet1
Sensing through Non-Sensing Ocular Ion Channels.
Kabra M et al.
International Journal of Molecular Sciences, 2020
Analysis of retinal structure and function in cone dystrophy with supernormal rod response.
Abdelkader E et al.
Documenta Ophthalmologica. Advances in Ophthalmology, 2020
KCNV2 retinopathy: clinical features, molecular genetics and directions for future therapy.
Guimaraes TAC et al.
Ophthalmic Genetics, 2020
32441199 (PubMed )
Supplement: IOPG_A_1766087_SM2520.pdf
'Cone dystrophy with supranormal rod response' in children.
Khan AO et al.
The British Journal of Ophthalmology, 2012
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