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Unusual clinical phenotype of Stargardt disease
Molina-Solana, Pedro; Morillo-Sánchez, María José; Méndez-Vidal, Cristina; Ramos-Jiménez, Manuel; Domínguez-Serrano, Borja; Antiñolo Gil, Guillermo; Rodríguez de la Rúa Franch, Enrique (2021)Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotypes have also been ...