Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect-Reference-Cited by-同舟云学术

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Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect

Published:2012-07 Issue:1 Volume:424 Page:152-157
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Ueyama Hisao,Muraki-Oda Sanae,Yamade Shinichi,Tanabe Shoko,Yamashita Takahiro,Shichida Yoshinori,Ogita Hisakazu

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference22 articles.

1. Tandem array of human visual pigment genes at Xq28;Vollrath;Science,1988

2. The evolution and physiology of human color vision: insights from molecular genetic studies of visual pigments;Nathans;Neuron,1999

3. Molecular genetics of human visual pigments;Nathans;Annu. Rev. Genet.,1992

4. Molecular genetics of inherited variation in human color vision;Nathans;Science,1986

5. Genotype–phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies;Deeb;Am. J. Hum. Genet.,1992

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