PubMed 27476654
Title: De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.
Authors:
Journal, date & volume: Am J Hum Genet, 2016Aug04, 99, 287-98
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/27476654
Abstract