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Article

Leber's hereditary optic neuropathy with molecular characterization in two Indian families.

Indian journal of ophthalmology - 1 Sept 2005

Verma I C, Bijarnia Sunita, Saxena Renu, Kohli Sudha, Puri Ratna Dua, Thomas Elizabeth, Chowdhary Debashish, Jha S N, Grover A K

Abstract excerpt

PURPOSE: Leber's hereditary optic neuropathy (LHON) presents in early adulthood with painless progressive blindness of one or both eyes. Usually there is a positive family history of similar disease on the maternal side. Definitive diagnosis can be established by finding the change in the mitochondrial gene. No molecular studies have been reported from India. MATERIAL AND METHODS: Clinical, ophthalmologic and...

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

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Identifiers

PMID: 16137960
DOI: 10.4103/0301-4738.16674

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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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