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Cause of hereditary blindness discovered
Date:6/22/2011

nterestingly, the CCDC66 protein is, for example, only localised in certain structures of the rods".

Studies continue

The insights gained from the studies of the working group can now be applied in order to better understand the processes that cause this inherited disorder. The mouse model will be studied further, as the researchers said: "with regard to malfunctions of the brain, but naturally, above all as a prerequisite for future therapeutic trials in retinitis pigmentosa."


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Contact: Professor Dr. Jrg Epplen
joerg.t.epplen@rub.de
49-023-432-23839
Ruhr-University Bochum
Source:Eurekalert

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