Clinical spectrum ofSCN1Amutations
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2009.02115.x/fullpdf
Reference25 articles.
1. De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study;Berkovic;Lancet Neurol,2006
2. Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy;Ceulemans;Pediatr Neurol,2004
3. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001
4. Mutation in the neuronal voltage gated sodium channel SCN1A in familial hemiplegic migraine;Dichgans;Lancet,2005
5. SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures;Ebach;Neuropediatrics,2005
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