Exploring mito-nuclear genetic factors in Leber's hereditary optic neuropathy: insights from comprehensive profiling of unique cases

Leber's hereditary optic neuropathy (LHON) is a mitochondrial complex I disorder and causes inexorable painless vision loss. Recent studies from India reported that a significant proportion of LHON patients lack primary mitochondrial DNA mutations, suggesting that alternative genetic factors co...

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Detalles Bibliográficos
Autores principales: Chermakani, Prakash, Gowri, Poigaialwar, Mahesh Kumar, Shanmugam, Sundaresan, Periasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694345/
http://dx.doi.org/10.17179/excli2023-6297

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694345/
http://dx.doi.org/10.17179/excli2023-6297

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