Mitochondrial Genetic Heterogeneity in Leber’s Hereditary Optic Neuropathy: Original Study with Meta-Analysis

Leber’s hereditary optic neuropathy (LHON) is a mitochondrial disorder that causes loss of central vision. Three primary variants (m.3460G>A, m.11778G>A, and m.14484T>C) and about 16 secondary variants are responsible for LHON in the majority of the cases. We investigated the complete mitoc...

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Detalles Bibliográficos
Autores principales: Jha, Rajan Kumar, Dawar, Chhavi, Hasan, Qurratulain, Pujar, Akhilesh, Gupta, Gaurav, Vishnu, Venugopalan Y., Kekunnaya, Ramesh, Thangaraj, Kumarasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472268/
https://www.ncbi.nlm.nih.gov/pubmed/34573281
http://dx.doi.org/10.3390/genes12091300

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472268/
https://www.ncbi.nlm.nih.gov/pubmed/34573281
http://dx.doi.org/10.3390/genes12091300

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