Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Cataract and GJA3[original query] |
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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 |
Use of high-throughput targeted exome sequencing in genetic diagnosis of Chinese family with congenital cataract. International journal of ophthalmology 2016 9 (5): 650-4. Ma Ming-Fu, Li Lian-Bing, Pei Yun-Qi, Cheng Z |
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 |
Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract. Eye (London, England) 2018 6 32 (10): 1661-1668. Berry Vanita, Ionides Alexander C W, Pontikos Nikolas, Moghul Ismail, Moore Anthony T, Cheetham Michael E, Michaelides Mich |
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 |
In silico analysis of non-synonymous single nucleotide polymorphisms (nsSNPs) in the human GJA3 gene associated with congenital cataract. BMC molecular and cell biology 2020 3 21 (1): 12. Zhang Mingzhou, Huang Chen, Wang Zhenyu, Lv Huibin, Li Xuem |
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