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Leber hereditary optic neuropathy: bridging the translational gap

PURPOSE OF REVIEW: Leber hereditary optic neuropathy (LHON) is the most common primary mitochondrial DNA (mtDNA) genetic disorder in the population. We address the clinical evolution of the disease, the secondary etiological factors that could contribute to visual loss, and the challenging task of d...

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Detalles Bibliográficos
Autores principales:	Jurkute, Neringa, Yu-Wai-Man, Patrick
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2017
Materias:	OCULAR GENETICS: Edited by Alex V. Levin
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562441/ https://www.ncbi.nlm.nih.gov/pubmed/28650878 http://dx.doi.org/10.1097/ICU.0000000000000410

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