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Article

Leber's hereditary optic neuropathy--the spectrum of mitochondrial DNA mutations in Chinese patients.

Japanese journal of ophthalmology - 1 Jan 2000

Yen May-Yung, Wang An-Guor, Chang Wei-Ling, Hsu Wen-Ming, Liu Jorn-Hon, Wei Yau-Huei

Abstract excerpt

PURPOSE: To investigate the spectrum of mitochondrial DNA (mtDNA) mutations in Chinese patients with Leber's hereditary optic neuropathy (LHON), optic atrophy of unknown etiology, and optic neuropathy of known etiology. METHODS: Twenty-seven patients from 25 LHON pedigrees, 22 patients with bilateral optic atrophy of unknown etiology, 21 patients with optic neuropathy of known etiology, and 25 normal healthy...

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Source

Identifiers

PMID: 11853713
DOI: 10.1016/s0021-5155(01)00460-9

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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