- SCN1A Gene Mutation and Adaptive Functioning in 18 Vietnamese Children with Dravet Syndrome
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Do TT, Vu DM, Huynh TT, Le TK, Sohn EH, Le TM, Ha HH, Bui CB
- KMID: 2364899
- J Clin Neurol.
- 2017 Jan;13(1):62-70.
- doi: 10.3988/jcn.2017.13.1.62
BACKGROUND AND PURPOSE: Dravet syndrome is a rare and severe type of epilepsy in infants. The heterogeneity in the overall intellectual disability that these patients suffer from has been attributed... -
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