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A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy
Iida, Kie, Ohkuma, Yasuhiro, Hayashi, Takaaki, Katagiri, Satoshi, Fujita, Takeshi, Tsunoda, Kazushige, Yamada, Hisashi, Tsuneoka, HiroshiLanguage:
english
Journal:
Ophthalmic Genetics
DOI:
10.3109/13816810.2015.1066829
Date:
February, 2016
File:
PDF, 738 KB
english, 2016