Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities

Vision Research

Volumn 73, Issue , 2012, Pages 1-9

  Baraas, Rigmor C ^a   Hagen, Lene A ^a   Dees, Elise W ^a   Neitz, Maureen ^b  

^a UNIVERSITY OF SOUTH EASTERN NORWAY   (Norway)

^b UNIVERSITY OF WASHINGTON   (United States)

Author keywords

Rod cone interaction; S opsin mutation; Tritan color vision deficiency

Indexed keywords

ISOLEUCINE; OPSIN; THREONINE;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; CLINICAL EVALUATION; COLOR DISCRIMINATION; COLOR VISION; COLOR VISION DEFECT; CONTROLLED STUDY; DARK ADAPTATION; FEMALE; GENETIC ASSOCIATION; GENOTYPE; HUMAN; LIGHT ADAPTATION; MALE; MUTATIONAL ANALYSIS; MUTATOR GENE; OPN1SW GENE; PRIORITY JOURNAL; RETINA CONE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; COLOR VISION; COLOR VISION DEFECTS; DARK ADAPTATION; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; ISOLEUCINE; MALE; MIDDLE AGED; MUTATION; PHENOTYPE; RETINA; ROD OPSINS; THREONINE; YOUNG ADULT;

EID: 84867324542     PISSN: 00426989     EISSN: 18785646     Source Type: Journal    
DOI: 10.1016/j.visres.2012.09.007     Document Type: Article

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