Showing results 5 to 6 of 6
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Title | Author(s) | Issue Date | |
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Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients Journal:Hong Kong Medical Journal | 2011 | ||
Movement disorders associated with thiamine pyrophosphokinase deficiency: Intrafamilial variability in the phenotype Journal:Clinical Neurology and Neurosurgery | 2020 |