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A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C MutationsA Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations
- Other Titles
- A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations
- Issue Date
- Apr-2020
- Publisher
- 대한신경과학회
- Citation
- Journal of Clinical Neurology, v.16, no.2, pp.338 - 340
- Journal Title
- Journal of Clinical Neurology
- Volume
- 16
- Number
- 2
- Start Page
- 338
- End Page
- 340
- ISSN
- 1738-6586
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - 의과대학 > 의학과 > 1. Journal Articles
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Related Researcher
- Lee, Jin Sook
- College of Medicine (Department of Medicine)