Yücel G, Yücel I, Bağci H, Aksu G, Lüleci G, Gümüşlü S, Aksu T A, Duranoğlu Y
Department of Biochemistry, Faculty of Medicine, Akdeniz University, Antalya, Türkiye.
Jpn J Ophthalmol. 1992;36(1):33-6.
No erythrocyte glucose-6-phosphate dehydrogenase (G6PD)-deficient person was detected among 90 male patients with congenital color blindness (CCB) diagnosed at the Ophthalmology Clinic of our Hospital. Eighteen complete G6PD-deficient subjects had normal color vision. These results suggest that there is a linkage disequilibrium between CCB and G6PD genes.
在我院眼科门诊确诊的90例先天性色盲（CCB）男性患者中，未检测到红细胞葡萄糖-6-磷酸脱氢酶（G6PD）缺乏者。18例完全G6PD缺乏者色觉正常。这些结果表明CCB与G6PD基因之间存在连锁不平衡。
