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- [43] Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations ORPHANET JOURNAL OF RARE DISEASES, 2017, 12 : 1 - 10
- [46] Identification of two novel OPA1 mutations in Chinese families with autosomal dominant optic atrophy MOLECULAR VISION, 2008, 14 (282): : 2451 - 2457