Novel mutations in the L visual pigment gene found in Japanese men with protan color-vision defect having a normal order L/M gene array-Reference-Cited by-同舟云学术

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Novel mutations in the L visual pigment gene found in Japanese men with protan color-vision defect having a normal order L/M gene array

Published:2016-03-11 Issue:4 Volume:37 Page:471-472
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Muraki Sanae¹,Ueyama Hisao²,Tanabe Shoko³,Yamade Shinichi¹,Ogita Hisakazu²,Ohji Masahito¹

Affiliation:

1. Department of Ophthalmology, Shiga University of Medical Science, Seta, Otsu, Japan

2. Department of Biochemistry and Molecular Biology, Shiga University of Medical Science, Seta, Otsu, Japan

3. Institute of Vision Research, Atsuta-ku, Nagoya, Japan

Funder

Japan Society for the Promotion of Science

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.3109/13816810.2015.1120319

Reference10 articles.

1. Molecular Genetics of Human Color Vision: The Genes Encoding Blue, Green, and Red Pigments

2. Molecular Genetics of Inherited Variation in Human Color Vision

3. Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies

4. Analysis of L-cone/M-cone visual pigment gene arrays in Japanese males with protan color-vision deficiency

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

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