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Wilbur C, Buerki SE, Guella I, Toyota EB, et al. An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2. Pediatr Neurol 2017 Jun 8. pii: S0887-8994(16)30708.
PMID: 28811059


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