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Mitochondrial DNA
The Journal of DNA Mapping, Sequencing, and Analysis
Volume 26, 2015 - Issue 2
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Short Communication

The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia

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Pages 208-212 | Received 24 Dec 2013, Accepted 15 Mar 2014, Published online: 08 Apr 2014

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Anastasia I Ryzhkova, Margarita A Sazonova, Vasily V Sinyov, Elena V Galitsyna, Mariya M Chicheva, Alexandra A Melnichenko, Andrey V Grechko, Anton Yu Postnov, Alexander N Orekhov & Tatiana P Shkurat. (2018) Mitochondrial diseases caused by mtDNA mutations: a mini-review. Therapeutics and Clinical Risk Management 14, pages 1933-1942.
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Omar Solyman & Peter MacIntosh. (2019) Leber Hereditary Optic Neuropathy in a Mother and Daughter Associated With m.10197G>A Mutation. Journal of Neuro-Ophthalmology 39:1, pages 142-142.
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Jin Sook LeeHunmin KimByung Chan LimHee HwangJieun ChoiKi Joong KimYong Seung HwangJong-Hee Chae. (2016) Leigh Syndrome in Childhood: Neurologic Progression and Functional Outcome. Journal of Clinical Neurology 12:2, pages 181.
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