Pickrell, O., Myers, C., McMahon, J., Schneider, A., Petrovski, S., Allen, A., . . . Mefford, H. (2016). De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies. The American Journal of Human Genetics, 99(2), pp. 287-298. doi:10.1016/j.ajhg.2016.06.003

Pickrell, Owen, et al. "De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies." The American Journal of Human Genetics 99, no. 2 (2016): 287-298.

Pickrell, Owen, et al. "De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies." The American Journal of Human Genetics 99.2 (2016): 287-298.