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The project aims to develop a cost effective method of examining the entire ABCA4 gene to look for variations that might cause disease.
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The project aims to develop a cost effective method of examining the entire ABCA4 gene to look for variations that might cause disease.
In February 2022, ProQR announced a disappointing outcome for their phase 2/3 trial of sepofarsen for Leber congenital amaurosis type 10 (LCA10).
It was previously believed that female carriers of X-linked inherited retinal diseases (IRDs) like X-linked retinitis pigmentosa (RP and Choroideremia) remained unaffected by sight loss.
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Inherited retinal dystrophies (IRDs) are the leading cause of blindness in working-age people in the UK, and children as young as eighteen-months are regularly diagnosed.
The collective partnership of eight of the leading charities in the sight loss sector, known for the last three years as the VI Charity Sector Partnership, has re-launched under a new identity of the ‘Vision Partnership’ with a re-invigorated purpose and new strategic focus.
Sepul Bio begins clinical trial of ultevursen for USH2A-associated RP
Research determines that taking high dose vitamin A supplements does not slow vision loss in people with retinitis pigmentosa (RP).