Title: Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy.

Authors: S D J Pena, R L M Coimbra

Journal, date & volume: Clin. Genet., 2015 Feb , 87, e1-3

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/25477152

Abstract