Pathogenic mitochondrial DNA mutations and associated clinical features in Korean patients with Leber's hereditary optic neuropathy

To identify the spectrum of pathogenic mitochondrial DNA (mtDNA) mutations and clinical features in Korean patients with genetically confirmed Leber's hereditary optic neuropathy (LHON). The medical records of 34 unrelated, genetically confirmed LHON patients were reviewed. Total genomic DNA wa...

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Veröffentlicht in:Investigative ophthalmology & visual science 2014-10, Vol.55 (12), p.8095-8101
Hauptverfasser: Yum, Hae Ri, Chae, Hyojin, Shin, Sun Young, Kim, Yonggoo, Kim, Myungshin, Park, Shin Hae
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Sprache:eng
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