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15. ABCA4 mutational spectrum in Mexican patients with Stargardt disease: Identification of 12 novel mutations and evidence of a founder effect for the common p.A1773V mutation. Chacón-Camacho OF; Granillo-Alvarez M; Ayala-Ramírez R; Zenteno JC Exp Eye Res; 2013 Apr; 109():77-82. PubMed ID: 23419329 [TBL] [Abstract][Full Text] [Related]