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4. The Clinical Features and Genetic Spectrum of a Large Cohort of Chinese Patients With Vitelliform Macular Dystrophies. Xuan Y; Zhang Y; Zong Y; Wang M; Li L; Ye X; Liu W; Chen J; Sun X; Zhang Y; Chen Y Am J Ophthalmol; 2020 Aug; 216():69-79. PubMed ID: 32278767 [TBL] [Abstract][Full Text] [Related]
5. Mutations in IMPG1 cause vitelliform macular dystrophies. Manes G; Meunier I; Avila-Fernández A; Banfi S; Le Meur G; Zanlonghi X; Corton M; Simonelli F; Brabet P; Labesse G; Audo I; Mohand-Said S; Zeitz C; Sahel JA; Weber M; Dollfus H; Dhaenens CM; Allorge D; De Baere E; Koenekoop RK; Kohl S; Cremers FP; Hollyfield JG; Sénéchal A; Hebrard M; Bocquet B; Ayuso García C; Hamel CP Am J Hum Genet; 2013 Sep; 93(3):571-8. PubMed ID: 23993198 [TBL] [Abstract][Full Text] [Related]
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9. Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2. Subash M; Rotsos T; Wright GA; Devery S; Holder GE; Robson AG; Pal B; Tufail A; Webster AR; Moore AT; Michaelides M Br J Ophthalmol; 2012 May; 96(5):719-22. PubMed ID: 22174098 [TBL] [Abstract][Full Text] [Related]
10. "Novel p.Tyr284Cys BEST1 genotype-phenotype correlations of Vitelliform Macular Dystrophy in a family with incomplete penetrance". Garza-Garza LA; León-Cachón RBR; Aguirre-Garza M; Garza-Leon M Ophthalmic Genet; 2020 Apr; 41(2):183-188. PubMed ID: 32207364 [No Abstract] [Full Text] [Related]
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12. Variants of BEST1 and CRYBB2 cause a complex ocular phenotype comprising microphthalmia, microcornea, cataract, and vitelliform macular dystrophy: case report. Shi J; Sun T; Xu K; Zhang X; Li Y BMC Ophthalmol; 2023 Apr; 23(1):165. PubMed ID: 37076855 [TBL] [Abstract][Full Text] [Related]
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16. Novel Mutation in BEST1 Associated with Atypical Best Vitelliform Dystrophy. Matson ME; Ly SV; Monarrez JL Optom Vis Sci; 2015 Aug; 92(8):e180-9. PubMed ID: 26099059 [TBL] [Abstract][Full Text] [Related]
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