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

Scientific reports - 8 Mar 2024

Yang Hee Kyung, Seong Moon-Woo, Hwang Jeong-Min

Abstract excerpt

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 the peripheral blood leukocytes of the patients with suspected LHON, and mtDNA mutations were identified by direct sequencing....

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Identifiers

PMID: 38459091
DOI: 10.1038/s41598-024-56215-x
PMCID: PMC10923793

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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