The findings of optical coherence tomography of retinal degeneration in relation to the morphological and electroretinographic features in RPE65−/− mice
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference44 articles.
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2. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy;SM Gu;Nat Genet,1997
3. Mutations in RPE65 cause Leber’s congenital amaurosis;F Marlhens;Nat Genet,1997
4. Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene;F Marlhens;Eur J Hum Genet,1998
5. Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa;H Morimura;Pro Natl Acad Sci USA,1998
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