CCDC102B confers risk of low vision and blindness in high myopia

• المؤلفون الرئيسيون: Hosoda, Y, Yoshikawa, M, Miyake, M, Tabara, Y, Shimada, N, Zhao, W, Oishi, A, Nakanishi, H, Hata, M, Akagi, T, Ooto, S, Nagaoka, N, Fang, Y, Kawaguchi, T, Setoh, K, Takahashi, Y, Kosugi, S, Nakayama, T, Ohno-Matsui, K, Cheng, C.-Y, Saw, S.M, Yamada, R, Matsuda, F, Tsujikawa, A, Yamashiro, K
• مؤلفون آخرون: SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
• التنسيق: مقال
• منشور في: Nature Publishing Group 2020
• الموضوعات: blindness; disease incidence; eye disease; gene; genome; risk; vision; Article; CCDC102B gene; choroid; ethnicity; gene expression; gene replication; genetic risk; genetic susceptibility; genome-wide association study; high myopia; human; intron; low vision; retina maculopathy; retinal pigment epithelium; risk assessment; single nucleotide polymorphism; adult; aged; Asian continental ancestry group; cohort analysis; complication; ethnology; female; genetic predisposition; genetics; Japan; male; metabolism; middle aged; myopia; pathology; retina macula lutea; Adult; Aged; Asian Continental Ancestry Group; Blindness; Choroid; Cohort Studies; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Macula Lutea; Male; Middle Aged; Myopia; Polymorphism, Single Nucleotide; Retinal Pigment Epithelium; Vision, Low
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/178414

10.1038/s41467-018-03649-3