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Dive into the research topics of 'A missense mutation in GUCY2D acts as a genetic modifier in RPE65-related Leber congenital amaurosis'. Together they form a unique fingerprint.- Sort by
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Eduardo Silva, Sharola Dharmaraj, Ying Ying Li, Ana Luisa Pina, Robert Colin Carter, Magali Loyer, Elias Traboulsi, George Theodossiadis, Robert K. Koenekoop, Olof H. Sundin, Irene H. Maumenee
Research output: Contribution to journal › Article › peer-review