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Visual function in patients with cone-rod dystrophy (CRD) associated with ABCR gene mutations

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Abstract

Mutations in the ABCR gene cause recessive Stargardt disease. In this study, we investigate the possibility that mutations in ABCR are associated with recessive cone- rod dystrophy (CRD) and use psychophysical, electroretinographic, and pupillometric techniques to characterize the phenotype.

© 2000 Optical Society of America

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