Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Blindness and NYX[original query] |
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Mutations in NYX of individuals with high myopia, but without night blindness. Molecular vision 2007 13 (): 330-6. Zhang Qingjiong, Xiao Xueshan, Li Shiqiang, Jia Xiaoyun, Yang Zhikuan, Huang Shizhou, Caruso Rafael C, Guan Tianqin, Sergeev Yuri, Guo Xiangming, Hejtmancik J Fieldi |
Genotyping microarray for CSNB-associated genes. Investigative ophthalmology & visual science 2009 Dec 50 (12): 5919-26. Zeitz Christina, Labs Stephan, Lorenz Birgit, Forster Ursula, Uksti Janne, Kroes Hester Y, De Baere Elfride, Leroy Bart P, Cremers Frans P M, Wittmer Mariana, van Genderen Maria M, Sahel José-Alain, Audo Isabelle, Poloschek Charlotte M, Mohand-Saïd Saddek, Fleischhauer Johannes C, Hüffmeier Ulrike, Moskova-Doumanova Veselina, Levin Alex V, Hamel Christian P, Leifert Dorothee, Munier Francis L, Schorderet Daniel F, Zrenner Eberhart, Friedburg Christoph, Wissinger Bernd, Kohl Susanne, Berger Wolfga |
A novel missense mutation in the NYX gene associated with high myopia. Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) 2013 May 33 (3): 346-53. Yip Shea Ping, Li Choi Chu, Yiu Wai Chi, Hung Wing Hong, Lam Wai Wa, Lai Man Chi, Ng Po Wah, Fung Wai Yan, Chu Patrick H W, Jiang Bo, Chan Henry H L, Yap Maurice K |
NYX mutations in four families with high myopia with or without CSNB1. Molecular vision 2015 21 213-23. Zhou Lin, Li Tuo, Song Xiusheng, Li Yin, Li Hongyan, Dan Hando |
Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness. Ophthalmic genetics 2016 Jul 1-5. Dan Handong, Song Xiusheng, Li Jiazhang, Xing Yiqiao, Li T |
Disinhibition of intrinsic photosensitive retinal ganglion cells in patients with X-linked congenital stationary night blindness. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2019 4 257 (6): 1207-1215. Schatz Andreas, Kelbsch Carina, Zeitz Christina, Kohl Susanne, Zrenner Eberhart, Gekeler Florian, Wilhelm Helmut, Wilhelm Barbara, Willmann Gabri |
Genetic Analysis of Consanguineous Pakistani Families with Congenital Stationary Night Blindness. Ophthalmic research 2021 11 65 (1): 104-110. Azhar Baig Hafiz Muhammad, Ansar Muhammad, Iqbal Afia, Naeem Muhammad Asif, Quinodoz Mathieu, Calzetti Giacomo, Iqbal Muhammad, Rivolta Car |
Congenital Stationary Night Blindness: Clinical and Genetic Features. International journal of molecular sciences 2022 12 23 (23): . Kim Angela H, Liu Pei-Kang, Chang Yin-Hsi, Kang Eugene Yu-Chuan, Wang Hung-Hsuan, Chen Nelson, Tseng Yun-Ju, Seo Go Hun, Lee Hane, Liu Laura, Chao An-Ning, Chen Kuan-Jen, Hwang Yih-Shiou, Wu Wei-Chi, Lai Chi-Chun, Tsang Stephen H, Hsiao Meng-Chang, Wang Nan-K |
HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis. Retina (Philadelphia, Pa.) 2023 12 44 (1): 117-126. Li Huang, Yanting Lai, Limei Sun, Songshan Li, Xiaoyan Di |
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- Page last updated:Apr 16, 2024
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