Associated Papers
Clarification of undiagnosed ataxia using whole-exome sequencing with clinical implications.
Kim M et al.
Parkinsonism & Related Disorders, 2020
Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes.
Lee CG et al.
Plos One, 2018
Genes and molecular mechanisms involved in the epileptogenesis of idiopathic absence epilepsies.
Yalçın O
Seizure, 2012
Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online.
Singh B et al.
Human Mutation, 2007
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