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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Detalles Bibliográficos
Autores principales: Mishra, Anushree, Devi, Saranya, Saxena, Rohit, Gupta, Neerja, Kabra, Madhulika, Chowdhury, Madhumita Roy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700584/
https://www.ncbi.nlm.nih.gov/pubmed/29133642
http://dx.doi.org/10.4103/ijo.IJO_380_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700584/
https://www.ncbi.nlm.nih.gov/pubmed/29133642
http://dx.doi.org/10.4103/ijo.IJO_380_17

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