A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy
オープンアクセス
書誌事項
- タイトル
- A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy
- 著者
- Iida K, Ohkuma Y, Hayashi T, Katagiri S, Fujita T, Tsunoda K，Yamada H, Tsuneoka H
収録刊行物
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- Ophthalmic Genet
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Ophthalmic Genet 37 354-6, 2016