The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy
<p>Maternally-inherited mitochondrial DNA (mtDNA) mutations cause symptoms of Leber’s hereditary optic neuropathy (LHON) in~ 1 in 30,000 individuals. Most of the affected individuals lack respiratory chain defects and there is no proven prophylactic treatment.</p> <p>We identified...
Main Authors: | , , , , , , , , , , , , , , , , , , |
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Format: | Journal article |
Published: |
American Association of Neurology
2016
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