Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Night Blindness and TRPM1[original query] |
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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 |
TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations. Scientific reports 2019 8 9 (1): 12047. AlTalbishi Alaa, Zelinger Lina, Zeitz Christina, Hendler Karen, Namburi Prasanthi, Audo Isabelle, Sheffer Ruth, Yahalom Claudia, Khateb Samer, Banin Eyal, Sharon Dr |
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 |
Phenotypes and genotypes underlying paradoxical pupillary reaction in children. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus 2022 6 26 (4): 205-207. Khan Arif |
Clinical and genetic findings in TRPM1-related congenital stationary night blindness. Acta ophthalmologica 2022 5 100 (6): e1332-e1339. Iosifidis Christos, Liu Jingshu, Gale Theodora, Ellingford Jamie M, Campbell Christopher, Ingram Stuart, Chandler Kate, Parry Neil R A, Black Graeme C, Sergouniotis Panagiotis |
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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