Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.

MLA

Everett, Kate, et al. “Linkage and Mutational Analysis of CLCN2 in Childhood Absence Epilepsy.” Epilepsy Research, vol. 75, no. 2–3, July 2007, pp. 145–53. EBSCOhost, https://doi.org/10.1016/j.eplepsyres.2007.05.004.

APA

Everett, K., Chioza, B., Aicardi, J., Aschauer, H., Brouwer, O., Callenbach, P., Covanis, A., Dooley, J., Dulac, O., Durner, M., Eeg-Olofsson, O., Feucht, M., Friis, M., Guerrini, R., Heils, A., Kjeldsen, M., Nabbout, R., Sander, T., Wirrell, E., … Gardiner, M. (2007). Linkage and mutational analysis of CLCN2 in childhood absence epilepsy. Epilepsy Research, 75(2–3), 145–153. https://doi.org/10.1016/j.eplepsyres.2007.05.004

Chicago

Everett, Kate, Barry Chioza, Jean Aicardi, Harald Aschauer, Oebele Brouwer, Petra Callenbach, Athanasios Covanis, et al. 2007. “Linkage and Mutational Analysis of CLCN2 in Childhood Absence Epilepsy.” Epilepsy Research 75 (2–3): 145–53. doi:10.1016/j.eplepsyres.2007.05.004.