Identification of two novel OPA1 mutations in Chinese families with autosomal dominant optic atrophy .2 .童绎. Leber病/ /王鸿启.现代神经眼科学.北京:人民卫生出版社,2005,118-125.3 .童绎,魏世辉,游世维.视路疾病的基础和临床进展.北京:人民卫生出版社,2010.4 .裴琼华,童绎.家族性视神经萎缩疾病的遗传分析.遗传学报,1979,6:166-168.5 .张丽珊,黄鹰,李方 ......