Literature DB >> 9893850

Molecular genetic detection of female carriers of protan defects.

P M Kainz1, M Neitz, J Neitz.   

Abstract

Females heterozygous for congenital colour vision defects are of interest because they are believed to have cone photoreceptor ratios and cone photopigments that differ from normal. We describe a molecular genetic method to identify protan carriers that involves characterizing the genes that occur in the most upstream position in each of the X-chromosome photopigment gene arrays.

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Year:  1998        PMID： 9893850     DOI： 10.1016/s0042-6989(97)00366-0

Source DB:  PubMed          Journal:  Vision Res        ISSN： 0042-6989            Impact factor:   1.886


  6 in total

1.  The L:M cone ratio in males of African descent with normal color vision.

Authors:  Carrie McMahon; Joseph Carroll; Stella Awua; Jay Neitz; Maureen Neitz
Journal:  J Vis       Date:  2008-02-20       Impact factor: 2.240

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

Authors:  Rigmor C Baraas; Lene A Hagen; Elise W Dees; Maureen Neitz
Journal:  Vision Res       Date:  2012-09-26       Impact factor: 1.886

3.  Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope.

Authors:  Maureen Neitz; Joseph Carroll; Agnes Renner; Holger Knau; John S Werner; Jay Neitz
Journal:  Vis Neurosci       Date:  2004 May-Jun       Impact factor: 3.241

4.  Protanomaly without darkened red is deuteranopia with rods.

Authors:  Steven K Shevell; Yang Sun; Maureen Neitz
Journal:  Vision Res       Date:  2008-04-18       Impact factor: 1.886

5.  Gene conversion and purifying selection shape nucleotide variation in gibbon L/M opsin genes.

Authors:  Tomohide Hiwatashi; Akichika Mikami; Takafumi Katsumura; Bambang Suryobroto; Dyah Perwitasari-Farajallah; Suchinda Malaivijitnond; Boripat Siriaroonrat; Hiroki Oota; Shunji Goto; Shoji Kawamura
Journal:  BMC Evol Biol       Date:  2011-10-22       Impact factor: 3.260

6.  Genetic Testing as a New Standard for Clinical Diagnosis of Color Vision Deficiencies.

Authors:  Candice Davidoff; Maureen Neitz; Jay Neitz
Journal:  Transl Vis Sci Technol       Date:  2016-09-06       Impact factor: 3.283
  6 in total

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