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6. Characterization of Ribozymes Targeting a Congenital Night Blindness Mutation in Rhodopsin Mutation. Conley SM; Whalen P; Lewin AS; Naash MI Adv Exp Med Biol; 2016; 854():509-15. PubMed ID: 26427453 [TBL] [Abstract][Full Text] [Related]
7. 1 rhodopsin mutations in congenital night blindness. McAlear SD; Kraft TW; Gross AK Adv Exp Med Biol; 2010; 664():263-72. PubMed ID: 20238025 [TBL] [Abstract][Full Text] [Related]
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9. Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. Rao VR; Cohen GB; Oprian DD Nature; 1994 Feb; 367(6464):639-42. PubMed ID: 8107847 [TBL] [Abstract][Full Text] [Related]
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14. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness. Bijveld MM; Florijn RJ; Bergen AA; van den Born LI; Kamermans M; Prick L; Riemslag FC; van Schooneveld MJ; Kappers AM; van Genderen MM Ophthalmology; 2013 Oct; 120(10):2072-81. PubMed ID: 23714322 [TBL] [Abstract][Full Text] [Related]
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18. Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohort. Malaichamy S; Sen P; Sachidanandam R; Arokiasamy T; Lancelot ME; Audo I; Zeitz C; Soumittra N Mol Vis; 2014; 20():341-51. PubMed ID: 24715752 [TBL] [Abstract][Full Text] [Related]
19. Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer. Al Oreany AA; Al Hadlaq A; Schatz P Graefes Arch Clin Exp Ophthalmol; 2016 Oct; 254(10):1951-1956. PubMed ID: 27084085 [TBL] [Abstract][Full Text] [Related]