PRRT2: A major cause of infantile epilepsy and other paroxysmal disorders of childhood
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Elsevier
Reference63 articles.
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2. PRRT2-related disorders: further PKD and ICCA cases and review of the literature;Becker;J. Neurol.,2013
3. A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16;Bennett;Neurology,2000
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1. Exploring epileptic phenotypes in PRRT2-related disorders: A report of two cases and literature appraisal;Seizure: European Journal of Epilepsy;2024-07
2. Heterozygous KCNJ10 variants affecting Kir4.1 channel cause paroxysmal kinesigenic dyskinesia;2023-09-01
3. ILAE Genetic Literacy Series: Self‐limited familial epilepsy syndromes with onset in neonatal age and infancy;Epileptic Disorders;2023-06-22
4. Synaptopathies in Developmental and Epileptic Encephalopathies: A Focus on Pre-synaptic Dysfunction;Frontiers in Neurology;2022-03-08
5. PRRT2 mutation in a Japanese woman: Adult-onset focal epilepsy coexisting with movement disorders and cerebellar atrophy;Epilepsy & Behavior Reports;2022
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