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4. Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders. Thiadens AA; den Hollander AI; Roosing S; Nabuurs SB; Zekveld-Vroon RC; Collin RW; De Baere E; Koenekoop RK; van Schooneveld MJ; Strom TM; van Lith-Verhoeven JJ; Lotery AJ; van Moll-Ramirez N; Leroy BP; van den Born LI; Hoyng CB; Cremers FP; Klaver CC Am J Hum Genet; 2009 Aug; 85(2):240-7. PubMed ID: 19615668 [TBL] [Abstract][Full Text] [Related]
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9. A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene. Chang B; Grau T; Dangel S; Hurd R; Jurklies B; Sener EC; Andreasson S; Dollfus H; Baumann B; Bolz S; Artemyev N; Kohl S; Heckenlively J; Wissinger B Proc Natl Acad Sci U S A; 2009 Nov; 106(46):19581-6. PubMed ID: 19887631 [TBL] [Abstract][Full Text] [Related]
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