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Your generous support allows Retina UK to fund the work of leading scientists who are increasing understanding of inherited sight loss and moving us closer to treatments.
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Your generous support allows Retina UK to fund the work of leading scientists who are increasing understanding of inherited sight loss and moving us closer to treatments.
Mirugen – Unlocking the Power of Retina Regeneration
Whether you're an expert runner, or a rebel *with* a cause, there's no better experience than the London Marathon!
The project aims to develop a cost effective method of examining the entire ABCA4 gene to look for variations that might cause disease.
SalioGen Developing Novel Gene Insertion Therapy for Stargardt disease.
The team have found the cause of disease in the first ever family tree drawn up at Moorfields Eye Hospital over 35 years ago, which had remained unsolved until now.
Choroideremia is a rare genetic condition resulting in progressive sight loss in men.
Autoimmune diseases are quite distinct from inherited retinal dystrophies.
The following projects were being funded by Retina UK and have recently come to an end.
This page explains the different types of genetic tests: diagnostic testing, predictive testing, carrier testing and research testing