Associated Papers
Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies.
Malechka VV et al.
Genes, 2022
RGR variants in different forms of retinal diseases: The undetermined role of truncation mutations.
Li J et al.
Molecular Medicine Reports, 2016
Assessment of computational methods for predicting the effects of missense mutations in human cancers.
Gnad F et al.
Bmc Genomics, 2013
23819521 (PubMed )
Supplement: 1471-2164-14-S3-S7-S1.xlsx › dbSNP
Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.
Morimura H et al.
Nature Genetics, 1999
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