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Gui, W. et al. (n.d.). NOVEL CONE DYSTROPHY WITH CENTRAL ELLIPSOID ZONE LOSS ASSOCIATED WITH HUMAN RETINAL FASCIN GENE (FSCN2) MUTATION. Retinal cases & brief reports. p. . [Online].
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Gui, W. et al. (n.d.). NOVEL CONE DYSTROPHY WITH CENTRAL ELLIPSOID ZONE LOSS ASSOCIATED WITH HUMAN RETINAL FASCIN GENE (FSCN2) MUTATION. Retinal cases & brief reports. p. . [Online].