- Leigh Syndrome: Subgroup Aanalysis according to Mitochondrial DNA Mutation
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Jee NL, Her SM, Kim SH, Lee MJ, Lee CH, Lee YM
- KMID: 2435267
- J Korean Child Neurol Soc.
- 2018 Mar;26(1):7-12.
- doi: 10.26815/jkcns.2018.26.1.7
PURPOSE: Leigh syndrome (LS) is a rare, progressive neurodegenerative disorder with characteristic abnormalities in the central nervous system. Such patients present with heterogeneous clinical symptoms and genetic abnormalities; thus, prognosis... -
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