Abstract
Leber’s hereditary optic neuropathy (LHON) is a maternal genetic disorder caused by point mutations of mitochondrial DNA (mtDNA). Visual field damage in LHON is mostly central defects of various sizes and shapes. In this section, several selected cases of the mutation of the same mtDNA are analyzed, and the pathogenesis of LHON is discussed at the molecular level.
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References
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© 2019 Springer Nature Singapore Pte Ltd. & People's Medical Publishing House, PR of China
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Pan, X., Fan, N., Liu, X. (2019). The Visual Field Defects of Leber’s Disease. In: Wang, N., Liu, X., Fan, N. (eds) Optic Disorders and Visual Field. Advances in Visual Science and Eye Diseases, vol 2. Springer, Singapore. https://doi.org/10.1007/978-981-13-2502-1_34
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DOI: https://doi.org/10.1007/978-981-13-2502-1_34
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