Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Retinitis Pigmentosa and CYP4V2[original query] |
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Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy. Experimental eye research 2016 Mar . Yin Xiaobei, Yang Liping, Chen Ningning, Cui Hui, Zhao Lin, Feng Lina, Li Aijun, Zhang Huirong, Ma Zhizhong, Li Genl |
Choroidal Vasculature in Bietti Crystalline Dystrophy With CYP4V2 Mutations and in Retinitis Pigmentosa With EYS Mutations. Investigative ophthalmology & visual science 2017 8 58 (10): 3871-3878. Hirashima Takako, Miyata Manabu, Ishihara Kenji, Hasegawa Tomoko, Sugahara Masako, Ogino Ken, Yoshikawa Munemitsu, Hata Masayuki, Kuroda Yoshimasa, Muraoka Yuki, Ooto Sotaro, Yoshimura Nagahi |
Mutation spectrum and genotype-phenotype correlation of inherited retinal dystrophy in Taiwan. Clinical & experimental ophthalmology 2019 Dec . Chen Zhen-Ji, Lin Keng-Hung, Lee Shi-Huang, Shen Ren-Juan, Feng Zhuo-Kun, Wang Xiao-Fang, Huang Xiu-Feng, Huang Zhi-Qin, Jin Zi-Bi |
Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort. Genes 2021 5 12 (5): . Kim Yoon-Jeon, Kim You-Na, Yoon Young-Hee, Seo Eul-Ju, Seo Go-Hun, Keum Changwon, Lee Beom-Hee, Lee Joo-Yo |
Genetic characteristics of suspected retinitis pigmentosa in a cohort of Chinese patients. Gene 2022 12 853 147087. Jin Bingyu, Li Jing, Yang Qiaodan, Tang Xinyu, Wang Chen, Zhao Yue, Zheng Fang, Zhang Yuanzhen, Ma Jianhong, Yan Mi |
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- Page last updated:Jun 24, 2024
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