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Article

Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population.

Indian journal of ophthalmology - 1 Nov 2017

Mishra Anushree, Devi Saranya, Saxena Rohit, Gupta Neerja, Kabra Madhulika, Chowdhury Madhumita Roy

Abstract excerpt

PURPOSE: Leber's hereditary optic neuropathy (LHON) is an inherited optic neuropathy characterized by subacute painless vision loss. The majority of LHON is caused due to one of the three primary mutations in the mitochondrial DNA (m.G3460A, m.G11778A, and m.T14484C). The frequency of these mutations differs in different populations. The purpose of this study is to observe the frequency of three common primary...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 29133642
DOI: 10.4103/ijo.IJO_380_17
PMCID: PMC5700584

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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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