共 50 条
- [22] A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family Scientific Reports, 4
- [24] First report of OPA1 screening in Greek patients with autosomal dominant optic atrophy and identification of a previously undescribed OPA1 mutation MOLECULAR VISION, 2014, 20 : 691 - 703
- [26] Optic atrophy and negative electroretinogram in a patient associated with a novel OPA1 mutation Graefe's Archive for Clinical and Experimental Ophthalmology, 2006, 244 : 274 - 275
- [30] A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family Journal of Neurology, 2015, 262 : 2323 - 2328