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) are an important cause of early vision loss and blindness. Among these, mutations in the PRPH2 gene are particularly common and affect up to 200,000 patients worldwide. However, PRPH2-related disease is highly
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Electro) Prof. Hyung-Soon Park (KAIST) The project is supported by clinical collaborators at Rigshospitalet and will involve joint supervision, regular biweekly meetings, and co-publication efforts
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(IRDs) are an important cause of early vision loss and blindness. Among these, mutations in the PRPH2 gene are particularly common and affect up to 200,000 patients worldwide. However, PRPH2-related
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