Literature DB >> 14121141

THE RED-LIGHT ABSOLUTE THRESHOLD IN HETEROZYGOTE PROTAN CARRIERS. POSSIBLE GENETIC IMPLICATIONS.

A E KRILL, E BEUTLER.   

Abstract

Keywords:  ADAPTATION, OCULAR; COLOR BLINDNESS; COLOR PERCEPTION; COLOR PERCEPTION TESTS; GENETICS, HUMAN

Mesh:

Year:  1964        PMID: 14121141

Source DB:  PubMed          Journal:  Invest Ophthalmol        ISSN: 0020-9988


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  5 in total

1.  Genetics of protan and deutan color-vision anomalies: an instructive family.

Authors:  H C Thuline; W E Hodgkin; G R Fraser; A G Motulsky
Journal:  Am J Hum Genet       Date:  1969-11       Impact factor: 11.025

2.  Mathematical models of retinitis pigmentosa: a study of the rate of progress in the different genetic forms.

Authors:  J T Pearlman
Journal:  Trans Am Ophthalmol Soc       Date:  1979

3.  [Evidence for reduced colour vision in carriers of congenital colour vision deficiencies (author's transl)].

Authors:  G Born; P Grützner; H Hemminger
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

4.  Richer color experience in observers with multiple photopigment opsin genes.

Authors:  K A Jameson; S M Highnote; L M Wasserman
Journal:  Psychon Bull Rev       Date:  2001-06

5.  Electroretinographic off-response in congenital red-green color deficiency and its genetic carrier.

Authors:  H Nakazato; H Hanazaki; K Kawasaki; J Tanabe; D Yonemura
Journal:  Doc Ophthalmol       Date:  1986-07-15       Impact factor: 2.379

  5 in total

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