Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Efficiency and USH2A[original query] |
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Microarray-based mutation analysis of 183 Spanish families with Usher syndrome. Investigative ophthalmology & visual science 2010 Mar 51 (3): 1311-7. Jaijo Teresa, Aller Elena, García-García Gema, Aparisi María J, Bernal Sara, Avila-Fernández Almudena, Barragán Isabel, Baiget Montserrat, Ayuso Carmen, Antiñolo Guillermo, Díaz-Llopis Manuel, Külm Maigi, Beneyto Magdalena, Nájera Carmen, Millán Jose |
MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome. Molecular vision 2015 1 20 1717-31. Sodi Andrea, Mariottini Alessandro, Passerini Ilaria, Murro Vittoria, Tachyla Iryna, Bianchi Benedetta, Menchini Ugo, Torricelli Frances |
Global spectrum of USH2A mutation in inherited retinal dystrophies: Prompt message for development of base editing therapy. Frontiers in aging neuroscience 2022 8 14 948279. Su Bing-Nan, Shen Ren-Juan, Liu Zhuo-Lin, Li Yang, Jin Zi-Bi |
Preimplantation genetic testing for hereditary hearing loss in Chinese population. Journal of assisted reproduction and genetics 2023 4 . Bi Qingling, Huang Shasha, Wang Hui, Gao Xue, Ma Minyue, Han Mingyu, Lu Sijia, Kang Dongyang, Nourbakhsh Aida, Yan Denise, Blanton Susan, Liu Xuezhong, Yuan Yongyi, Yao Yuanqing, Dai |
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- Page last updated:Dec 05, 2023
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