Vaccination management in an asymptomatic child with a novel SCN1A variant and family history of status epilepticus following vaccination: A case report on a potential new direction in personalised medicine
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology,General Medicine
Reference15 articles.
1. Genotype-phenotype associations in SCN1A-related epilepsies;Zuberi;Neurology,2011
2. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001
3. Genetic epilepsy with febrile seizures plus: refining the spectrum;Zhang;Neurology,2017
4. Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study;McIntosh;Lancet Neurol,2010
5. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology;Richards;Genet Med,2015
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