J Mov Disord.
2022 May;15(2):178-180. 10.14802/jmd.21139.
A Case of AOA2 With Compound Heterozygous SETX Mutations
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- 1Department of Neurology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea
- 2Department of Neurology, Inha University Hospital, Incheon, Korea
- 3Rare Disease Center, Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea
- 4Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea
- KMID: 2530227
- DOI: http://doi.org/10.14802/jmd.21139
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