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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 5, 2024. (Total: 232220Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Glaucoma and NTF4[original query]
Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population.
Molecular vision 2010 16 1640-5.
Vithana Eranga N, Nongpiur Monisha E, Venkataraman Divya, Chan Stephanie H, Mavinahalli Jagadeesh, Aung T
Variations in NTF4, VAV2, and VAV3 genes are not involved with primary open-angle and primary angle-closure glaucomas in an indian population.
Investigative ophthalmology & visual science 2010 Oct 51 (10): 4937-41.
Rao Kollu N, Kaur Inderjeet, Parikh Rajul S, Mandal Anil K, Chandrasekhar Garudadri, Thomas Ravi, Chakrabarti Subhabra
No evidence of association of heterozygous NTF4 mutations in patients with primary open-angle glaucoma.
American journal of human genetics 2010 Mar 86 (3): 498-9; author reply 500.
Liu Yutao, Liu Wenjing, Crooks Kristy, Schmidt Silke, Allingham R Rand, Hauser Michael
WDR36 variants in East Indian primary open-angle glaucoma patients.
Molecular vision 2011 17 2618-27.
Mookherjee Suddhasil, Chakraborty Subhadip, Vishal Mansi, Banerjee Deblina, Sen Abhijit, Ray Kun
Association of eNOS polymorphisms with primary angle-closure glaucoma.
Investigative ophthalmology & visual science 2013 Mar 54 (3): 2108-14.
Awadalla Mona S, Thapa Suman S, Hewitt Alex W, Craig Jamie E, Burdon Kathryn
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
Detection of mutations in MYOC, OPTN, NTF4, WDR36 and CYP1B1 in Chinese juvenile onset open-angle glaucoma using exome sequencing.
Scientific reports 2018 Mar 8 (1): 4498.
Huang Chukai, Xie Lijing, Wu Zhenggen, Cao Yingjie, Zheng Yuqian, Pang Chi-Pui, Zhang Mingz
Mutation profile of glaucoma candidate genes in Mauritanian families with primary congenital glaucoma.
Molecular vision 2019 25 373-381.
Hadrami Mouna, Bonnet Crystel, Zeitz Christina, Veten Fatimetou, Biya Med, Hamed Cheikh T, Condroyer Christel, Wang Panfeng, Sidi Med Mahmoud, Cheikh Sidi, Zhang Qingjiong, Audo Isabelle, Petit Christine, Houmeida Ahm
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