Cite
DE NOVO LOSS- OR GAIN-OF-FUNCTION MUTATIONS IN KCNA2 CAUSE EPILEPTIC ENCEPHALOPATHY
MLA
Syrbe, S., et al. De Novo Loss- or Gain-Of-Function Mutations in Kcna2 Cause Epileptic Encephalopathy. 2015. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1247372437&authtype=sso&custid=ns315887.
APA
Syrbe, S., Hedrich, U., Riesch, E., Djemie, T., Mueller, S., Moller, R. S., Maher, B., Hernandez-Hernandez, L., Synofzik, M., Caglayan, H., Arslan, M., Serratosa, J., Nothnagel, M., May, P., Krause, R., Loeffler, H., Detert, K., Dorn, T., Vogt, H., … Lemke, J. (2015). De Novo Loss- or Gain-Of-Function Mutations in Kcna2 Cause Epileptic Encephalopathy.
Chicago
Syrbe, S., U. Hedrich, E. Riesch, T. Djemie, S. Mueller, R. S. Moller, B. Maher, et al. 2015. “De Novo Loss- or Gain-Of-Function Mutations in Kcna2 Cause Epileptic Encephalopathy.” http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1247372437&authtype=sso&custid=ns315887.