Loss of cone function in the central retina is a pivotal event in the development of severe vision impairment for many prevalent blinding diseases. Complete achromatopsia is a genetic defect resulting ...
Inherited retinal dystrophies are a heterogeneous group of disorders that nearly always share one critical feature, degeneration of photoreceptors. Retinal dystrophies often lead to blindness and ...
Laura Kelley receives funding from People Programme (Marie Curie Actions) of the European Union’s Seventh Framework Programme (FP7/2007-2013). As humans, we live in a colourful world, but differences ...
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