Pathophysiology of EIMFS: genetic in 69% of patients and involves processes from gene and protein regulation to ion channel function and solute trafficking

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Abstract

 OBJECTIVE:

Epilepsy of infancy with migrating focal seizures (EIMFS) is one of the most severe developmental and epileptic encephalopathies. We delineate the genetic causes and genotype-phenotype correlations of a large EIMFS cohort. 

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