Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Blindness and GRM6[original query] |
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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 |
Sequence variations of GRM6 in patients with high myopia. Molecular vision 2009 15 2094-100. Xu Xiaoyu, Li Shiqiang, Xiao Xueshan, Wang Panfeng, Guo Xiangming, Zhang Qingjio |
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 |
Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse. Equine veterinary journal 2020 7 53 (2): 316-323. Hack Yael L, Crabtree Elizabeth E, Avila Felipe, Sutton Roger B, Grahn Robert, Oh Annie, Gilger Brian, Bellone Rebecca |
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 |
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