Early mortality in SCN8A -related epilepsies
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference10 articles.
1. De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy;Blanchard;J. Med. Genet.,2015
2. Mortality in Dravet syndrome;Cooper;Epilepsy Res.,2016
3. Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation;Gardella;Ann. Neurol.,2016
4. SCN8A-related epilepsy with encephalopathy;Hammer,2018
5. SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability;Kong;Epilepsia,2015
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2. Global modified‐Delphi consensus on comorbidities and prognosis of SCN8A‐related epilepsy and/or neurodevelopmental disorders;Epilepsia;2024-05-27
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4. Beyond the Norm: A Report of a Rare Case of Sodium Channel 8 Alpha (SCN8A) Gene-Related Epilepsy Unveiled in a Nine-Year-Old Child;Cureus;2024-05-07
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