Ann Child Neurol.
2020 Jul;28(3):118-121. 10.26815/acn.2020.00024.
De Novo SCN8A Pathogenic Variant (c.5630A>G; p.Asn1877Ser) Presenting with a Relatively Mild Phenotype
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- 1Department of Pediatrics, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea
- 2GC Genome, Yongin, Korea
- KMID: 2504763
- DOI: http://doi.org/10.26815/acn.2020.00024
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