共 50 条
- [1] A novel mutation of the OPA1 gene in a Japanese patient with autosomal dominant optic atrophy Graefe's Archive for Clinical and Experimental Ophthalmology, 2007, 245 : 1581 - 1583
- [4] A novel mutation of the OPA1 gene responsible for isolated autosomal dominant optic atrophy in two brothers JOURNAL FRANCAIS D OPHTALMOLOGIE, 2007, 30 (02): : 161 - 164
- [6] A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy Journal of Neurology, 2006, 253 : 672 - 673
- [9] A Novel Missense OPA1 Mutation in a Patient with Dominant Optic Atrophy and Cervical Dystonia MOVEMENT DISORDERS CLINICAL PRACTICE, 2019, 6 (02): : 171 - 173