New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome-Reference-Cited by-同舟云学术

New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome

Published:2016-08-13 Issue:6 Volume:60 Page:476-485
ISSN:0021-5155
Container-title:Japanese Journal of Ophthalmology
language:en
Short-container-title:Jpn J Ophthalmol

Author:

Kuniyoshi Kazuki,Hayashi Takaaki,Sakuramoto Hiroyuki,Mishima Hiroshi,Tsuneoka Hiroshi,Tsunoda Kazushige,Iwata Takeshi,Shimomura Yoshikazu

Funder

Ministry of Education, Culture, Sports, Science and Technology, Japan

Japan Agency for Medical Research and Development

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s10384-016-0470-0.pdf

Reference51 articles.

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3. Jacobson SG, Marmor MF, Kemp CM, Knighton RW. SWS (blue) cone hypersensitivity in a newly identified retinal degeneration. Invest Ophthalmol Vis Sci. 1990;31:827–38.

4. Kellner U, Zrenner E, Sadowski B, Foerster MH. Enhanced S cone sensitivity syndrome: long-term follow-up, electrophysiological and psychophysical findings. Clin Vis Sci. 1993;8:425–34.

5. Pachydaki SI, Bhatnagar PA, Barbazetto IA, Klaver CC, Freund BK, Yannuzzi LA. Long-term follow-up in enhanced S-cone syndrome. Retin Cases Brief Rep. 2009;3:118–20.

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