Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/ RDS gene

• 家族性多代显性遗传中心性晕轮状脉络膜营养不良与外周蛋白/RDS基因上的精氨酸195亮氨酸突变相关的临床所见