HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia
10.1111/cge.12030
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| Main Author: | |
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| Format: | Editorial |
| Language: | English |
| Published: |
WILEY-BLACKWELL
2022
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| Online Access: | https://scholarbank.nus.edu.sg/handle/10635/235312 |
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| Institution: | National University of Singapore |
| Language: | English |