著者名,論文名,雑誌名,ISSN,出版者名,出版日付,巻,号,ページ,URL,URL(DOI)
,A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy,Ophthalmic Genet,,,2016,37,,354-6,https://cir.nii.ac.jp/crid/1010000782305993220,