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Exome sequencing to identify a de novo ATP1A3 mutation in motor neuron disease mimicking rapid onset dystonia Parkinsonism
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | 오기욱 | - |
| dc.date.accessioned | 2021-08-02T22:51:56Z | - |
| dc.date.available | 2021-08-02T22:51:56Z | - |
| dc.date.issued | 2017-11-11 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/30141 | - |
| dc.title | Exome sequencing to identify a de novo ATP1A3 mutation in motor neuron disease mimicking rapid onset dystonia Parkinsonism | - |
| dc.type | Conference | - |
| dc.citation.conferenceName | 2017년 추계 신경과학회 학술대회 | - |
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Collections - 서울 의과대학 > 서울 신경과학교실 > 2. Conference Papers
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Related Researcher
- Oh, Ki Wook
- 서울 의과대학 (DEPARTMENT OF NEUROLOGY)