A missense mutation in GUCY2D acts as a genetic modifier in RPE65-related Leber Congenital Amaurosis

Author: Silva Eduardo   Dharmaraj Sharola   Li Ying Ying   Pina Ana Luisa   Carter Robert Colin   Loyer Magali   Traboulsi Elias   Theodossiadis George   Koenekoop Robert   Sundin Olof   Maumenee Irene  

Publisher: Informa Healthcare

ISSN: 1381-6810

Source: Ophthalmic Genetics, Vol.25, Iss.3, 2004-09, pp. : 205-217

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Abstract