reference/19559328

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bibliographicCitation	Iida K, Ohkuma Y, Hayashi T, Katagiri S, Fujita T, Tsunoda K, Yamada H, Tsuneoka H. A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy. Ophthalmic Genet. 2016 Sep;37(3):354–6. doi: 10.3109/13816810.2015.1066829. PMID: 26854526.
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date	2016-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.3109/13816810.2015.1066829 https://pubmed.ncbi.nlm.nih.gov/26854526
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy
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