A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy

Open Access

Bibliographic Information

Title
A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy
Author
Iida K, Ohkuma Y, Hayashi T, Katagiri S, Fujita T, Tsunoda K，Yamada H, Tsuneoka H

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Details 詳細情報について

  • CRID
    1010000782305993220
  • Article Type
    journal article
  • Data Source
    • KAKEN

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