A high association with cone dystrophy fundus albipunctatus caused by mutations of the RDH5 gene

Investigative Ophthalmology and Visual Science

Volumn 41, Issue 12, 2000, Pages 3925-3932

  Nakamura, M ^a   Hotta, Y ^a   Tanikawa, A ^a   Terasaki, H ^a   Miyake, Y ^a  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; ARGININE; DNA; GLYCINE; HISTIDINE; METHIONINE; SERINE; VALINE;

ADOLESCENT; ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; CONE DYSTROPHY; ELECTRORETINOGRAPHY; EYE FUNDUS ALBIPUNCTATUS; FEMALE; FRAMESHIFT MUTATION; GENE AMPLIFICATION; GENE MUTATION; HUMAN; MALE; NIGHT BLINDNESS; OPHTHALMOSCOPY; PRIORITY JOURNAL; RETINA DISEASE; SEQUENCE ANALYSIS; SLIT LAMP; VISUAL ACUITY;

ADOLESCENT; ADULT; AGED; ALCOHOL OXIDOREDUCTASES; CHILD; CONES (RETINA); DNA MUTATIONAL ANALYSIS; ELECTRORETINOGRAPHY; FEMALE; FUNDUS OCULI; HUMANS; MALE; MIDDLE AGED; MUTATION; NIGHT BLINDNESS; OPHTHALMOSCOPY; PHOTOGRAPHY; POLYMERASE CHAIN REACTION; RETINAL DEGENERATION; VISUAL ACUITY;

EID: 0033765274     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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