Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy

Abstract In order to explore the spectrum of mitochondrial DNA (mtDNA) mutations in Korean patients with Leber's hereditary optic neuropathy (LHON), we investigated the spectrum of mtDNA mutations in 145 Korean probands confirmed with the diagnosis of LHON. Total genomic DNA was isolated from t...

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Bibliographic Details
Main Authors: Hee Kyung Yang, Moon-Woo Seong, Jeong-Min Hwang
Format: Article
Language:English
Published: Nature Portfolio 2024-03-01
Series:Scientific Reports
Subjects:
Online Access:https://doi.org/10.1038/s41598-024-56215-x