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

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

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 mut...

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Bibliographic Details
Main Authors: Anushree Mishra, Saranya Devi, Rohit Saxena, Neerja Gupta, Madhulika Kabra, Madhumita Roy Chowdhury
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Indian Journal of Ophthalmology
Subjects:
Homoplasmy
Leber's hereditary optic neuropathy
mitochondrial DNA
optic atrophy
primary mutation
Online Access:http://www.ijo.in/article.asp?issn=0301-4738;year=2017;volume=65;issue=11;spage=1156;epage=1160;aulast=Mishra

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http://www.ijo.in/article.asp?issn=0301-4738;year=2017;volume=65;issue=11;spage=1156;epage=1160;aulast=Mishra

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