Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Retinal Degeneration and Erg[original query] |
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[A study of PDE6B gene mutation and phenotype in Chinese cases with retinitis pigmentosa]. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2003 Jan 39 (1): 28-32. Cui Yun, Zhao Kan-xing, Wang Li, Wang Qing, Zhang Wei, Chen Wei-ying, Wang Li-mi |
SLC7A14 linked to autosomal recessive retinitis pigmentosa. Nature communications 2014 5 3517. Jin Zi-Bing, Huang Xiu-Feng, Lv Ji-Neng, Xiang Lue, Li Dong-Qing, Chen Jiangfei, Huang Changjiang, Wu Jinyu, Lu Fan, Qu J |
Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations. Molecular vision 2015 21 783-92. Sharon Dror, Banin Ey |
Association of CRX genotypes and retinal phenotypes confounded by variable expressivity and electronegative electroretinogram. Clinical & experimental ophthalmology 2020 3 48 (5): 644-657. Nishiguchi Koji M, Kunikata Hiroshi, Fujita Kosuke, Hashimoto Kazuki, Koyanagi Yoshito, Akiyama Masato, Ikeda Yasuhiro, Momozawa Yukihide, Sonoda Koh-Hei, Murakami Akira, Wada Yuko, Nakazawa To |
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