Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population

• المؤلفون الرئيسيون: Abu-Amero, K.K, Helwa, I, Al-Muammar, A, Strickland, S, Hauser, M.A, Allingham, R.R, Liu, Y
• مؤلفون آخرون: DUKE-NUS MEDICAL SCHOOL
• التنسيق: مقال
• منشور في: 2020
• الموضوعات: adult; allele; Article; case control study; central corneal thickness; COL5A1 gene; controlled study; disease predisposition; female; FNDC3B gene; FOXO1 gene; gene; gene mutation; genetic analysis; genetic association; genetic susceptibility; genetic variability; genotype; human; keratoconus; LCN12 PTGDS gene; major clinical study; male; population research; promoter region; risk factor; RXRA COL5A1 gene; Saudi Arabia; single nucleotide polymorphism; cornea; genetic association study; genetic variation; genetics; health survey; pathology; procedures; young adult; Adult; Case-Control Studies; Cornea; Female; Genetic Association Studies; Genetic Variation; Humans; Keratoconus; Male; Population Surveillance; Young Adult
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/181447

10.1186/s12952-015-0029-5