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bibliographicCitation Pesch UE, Leo-Kottler B, Mayer S, Jurklies B, Kellner U, Apfelstedt-Sylla E, Zrenner E, Alexander C, Wissinger B. OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance. Hum Mol Genet. 2001 Jun 15;10(13):1359–68. doi: 10.1093/hmg/10.13.1359. PMID: 11440988.
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title OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance
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