Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Cataract and GJA8[original query] |
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A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract. Molecular vision 2008 14 418-24. Yan Ming, Xiong Chenling, Ye Shui Qing, Chen Yongmei, Ke Min, Zheng Fang, Zhou X |
Association between gap junction protein-alpha 8 polymorphisms and age-related cataract. Molecular biology reports 2011 Feb 38 (2): 1301-7. Liu Yuanyuan, Ke Min, Yan Ming, Guo Shuren, Mothobi Mane Emily, Chen Qiang, Zheng Fa |
The KORA Eye Study: a population-based study on eye diseases in Southern Germany (KORA F4). Investigative ophthalmology & visual science 2011 Sep 52 (10): 7778-86. Graw Jochen, Welzl Gerhard, Ahmad Nafees, Klopp Norman, Heier Margit, Wulff Andrea, Heinrich Joachim, Döring Angela, Karrasch Stefan, Nowak Dennis, Schulz Holger, Rathmann Wolfgang, Illig Thomas, Peters Annette, Holle Rolf, Meisinger Christa, Wichmann H Eri |
Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study. Molecular vision 2011 17 621-6. Zhou Zhou, Wang Binbin, Hu Shanshan, Zhang Chunmei, Ma Xu, Qi Yanh |
Exome sequencing identifies a novel mutation in GJA8 associated with inherited cataract in a Chinese family. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2016 Oct . Ren Mei, Yang Xin Guang, Dang Xiao Jie, Xiao Jin |
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia. G3 (Bethesda, Md.) 2017 8 7 (10): 3257-3268. Javadiyan Shari, Craig Jamie E, Souzeau Emmanuelle, Sharma Shiwani, Lower Karen M, Mackey David A, Staffieri Sandra E, Elder James E, Taranath Deepa, Straga Tania, Black Joanna, Pater John, Casey Theresa, Hewitt Alex W, Burdon Kathryn |
Novel Mutations in the Crystallin Gene in Age-Related Cataract Patients from a North Indian Population. Molecular syndromology 2017 Jun 8 (4): 179-186. Patel Rashmi, Zenith Ravish K, Chandra Abhishek, Ali Akht |
Genetic investigation of ocular developmental genes in 52 patients with anophthalmia/microphthalmia. Ophthalmic genetics 2018 Feb 1-9. Vidya Nair Gopinathan, Rajkumar Sankaranarayanan, Vasavada Abhay |
The impact of GJA8 SNPs on susceptibility to age-related cataract. Human genetics 2018 Dec 137 (11-12): 897-904. Yu Xiaoning, Ping Xiyuan, Zhang Xin, Cui Yilei, Yang Hao, Tang Xiajing, Tang Yelei, Shentu Xingch |
Clinical and genetic findings in patients with congenital cataract and heart diseases. Orphanet journal of rare diseases 2021 6 16 (1): 242. Li Xinru, Si Nuo, Song Zixun, Ren Yaqiong, Xiao W |
[Analysis of novel compound heterozygous variants of the GJA8 gene in a child with congenital cataract]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 11 39 (11): 1262-1265. Li Ruirui, Xu Peiwen, Zou Yang, Li Jie, Gao Yu |
First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype Association. Journal of clinical medicine 2022 1 11 (1): . Stingl Julia V, Diederich Stefan, Diel Heidi, Schuster Alexander K, Wagner Felix M, Chronopoulos Panagiotis, Aghayeva Fidan, Grehn Franz, Winter Jennifer, Schweiger Susann, Hoffmann Esther |
Identification of a Missense Mutation in GJA8 Gene in an Iranian Family with Autosomal Dominant Congenital Cataract. Journal of current ophthalmology 2023 9 35 (1): 73-78. Mahla Asghari, Soheila Abedini, Melika Farshidianfar, Amir Tajbakhsh, Akbar Derakhshan, Alireza Pasd |
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- Page last updated:Apr 16, 2024
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