Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa

Nature Genetics

Volumn 23, Issue 4, 1999, Pages 393-394

  Morimura, Hiroyuki ^a   Saindelle Ribeaudeau, Florence ^b   Berson, Eliot L ^a   Dryja, Thaddeus P ^a  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^b CENTRE HOSPITALIER DU MANS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

11 CIS RETINAL; OPSIN; RETINAL; RHODOPSIN;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; ELECTRORETINOGRAM; FEMALE; GENE FREQUENCY; GENE MUTATION; GENE SEGREGATION; HUMAN; LEBER CONGENITAL AMAUROSIS; MALE; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA MACULA AGE RELATED DEGENERATION; RETINITIS PIGMENTOSA; SINGLE STRAND CONFORMATION POLYMORPHISM; SOUTHERN BLOTTING; VISUAL ACUITY;

AGED; EYE PROTEINS; FEMALE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; MUTATION; OPSIN; PEDIGREE; RECEPTORS, CELL SURFACE; RECEPTORS, G-PROTEIN-COUPLED; RETINITIS PIGMENTOSA;

EID: 0032708573     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/70496     Document Type: Article

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