Visual function in retinitis pigmentosa related to a codon 15 rhodopsin gene mutation

Ophthalmic Research

Volumn 30, Issue 1, 1998, Pages 1-10

  Yoshii, Masaru ^a   Murakami, Akira ^a   Akeo, Kiyoshi ^a   Fujiki, Keiko ^b   Saga, Masamichi ^d   Mizukawa, Atsushi ^a   Itoh, Junji ^a   Okisaka, Shigekuni ^a   Yanashima, Kenji ^c   Hotta, Yoshihiro ^b   Kanai, Atsushi ^b   Oguchi, Yoshihisa ^d  

^a NATIONAL DEFENSE MEDICAL COLLEGE   (Japan)

^b JUNTENDO UNIVERSITY   (Japan)

^c NATIONAL REHABILITATION CENTER FOR PERSONS WITH DISABILITIES   (Japan)

^d KEIO UNIVERSITY   (Japan)

Author keywords

Codon 15; Full field stimulus; Multifocal electroretinogram; Retinitis pigmentosa; Rhodopsin gene mutation

Indexed keywords

ASPARAGINE; RESTRICTION ENDONUCLEASE; RHODOPSIN; SERINE;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; CODON; CONTROLLED STUDY; DNA SEQUENCE; ELECTRORETINOGRAPHY; FEMALE; GENE MUTATION; HUMAN; JAPAN; MALE; PHENOTYPE; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; VISION; VISUAL FIELD DEFECT;

ADULT; AGED; CODON; DARK ADAPTATION; DNA; DNA PRIMERS; ELECTROPHORESIS, POLYACRYLAMIDE GEL; ELECTRORETINOGRAPHY; FEMALE; HUMANS; MALE; MIDDLE AGED; PEDIGREE; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; RETINITIS PIGMENTOSA; RHODOPSIN; VISION;

EID: 6844260558     PISSN: 00303747     EISSN: None     Source Type: Journal    
DOI: 10.1159/000055448     Document Type: Article

References (16)

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