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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