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Myers, Candace T, McMahon, Jacinta M, Schneider, Amy L, Petrovski, Slave, Allen, Andrew S, Carvill, Gemma L, Zemel, Matthew, Say-Kally, Julia E, LaCroix, Amy J, Heinzen, Erin L
et al (show 34 more authors) (2016) De Novo Mutations in <i>SLC1A2</i> and <i>CACNA1A</i> Are Important Causes of Epileptic Encephalopathies. AMERICAN JOURNAL OF HUMAN GENETICS, 99 (2). pp. 287-298.

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