Indications for Genetic Testing for Dravet Syndrome
DOI:
https://doi.org/10.15844/pedneurbriefs-25-11-7Keywords:
SCN1A Mutations, Genetic Testing, Dravet SyndromeAbstract
Researchers at the Cincinnati Children’s Medical Center, OH investigated the predictive value of features of Dravet syndrome, as defined by the International League Against Epilepsy, as criteria for a positive SCN1A gene mutation in a cohort of consecutively tested children.Published
2011-11-01
Issue
Section
Infectious/Autoimmune Disorders
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