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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 7, 2023. (Total: 223846Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Vision and OPA1[original query]
Mutation screening of mitochondrial DNA as well as OPA1 and OPA3 in a Chinese cohort with suspected hereditary optic atrophy.
Investigative ophthalmology & visual science 2014 Oct 55 (10): 6987-95.
Chen Jieqiong, Xu Ke, Zhang Xiaohui, Jiang Feng, Liu Lijuan, Dong Bing, Ren Yanfan, Li Ya
Mutation analysis of seven known glaucoma-associated genes in Chinese patients with glaucoma.
Investigative ophthalmology & visual science 2014 Jun 55 (6): 3594-602.
Huang Xiaobo, Li Miaoling, Guo Xiangming, Li Shiqiang, Xiao Xueshan, Jia Xiaoyun, Liu Xing, Zhang Qingjio
Polymorphism Analysis of GSTM1 and OPA1 Genes in Greek Patients with Primary Open-angle Glaucoma.
In vivo (Athens, Greece) 0 30 (4): 473-477.
Lavaris Anastasios, Gazouli Maria, Brouzas Dimitrios, Moschos Marilita
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families.
Journal of the neurological sciences 2017 11 382 29-35.
Pretegiani E, Rosini F, Rufa A, Gallus G N, Cardaioli E, Da Pozzo P, Bianchi S, Serchi V, Collura M, Franceschini R, Bianchi Marzoli S, Dotti M T, Federico
Meta-analysis of genotype-phenotype analysis of OPA1 mutations in autosomal dominant optic atrophy.
Mitochondrion 2018 8 46 262-269.
Ham Michelle, Han Julia, Osann Kathryn, Smith Moyra, Kimonis Virgin
Mitochondrial Mutations in Ethambutol-Induced Optic Neuropathy.
Frontiers in cell and developmental biology 2021 10 9 754676.
Zhang Xiao-Hui, Xie Yue, Xu Quan-Gang, Cao Kai, Xu Ke, Jin Zi-Bing, Li Yang, Wei Shi-H
Autosomal dominant optic atrophy caused by six novel pathogenic OPA1 variants and genotype-phenotype correlation analysis.
BMC ophthalmology 2022 7 22 (1): 322.
Han Jinfeng, Li Ya, You Ya, Fan Ke, Lei
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