APA
Larsen J., Johannesen K. M., Ek J., Tang S., Marini C., Blichfeldt S., Kibaek M., von Spiczak S., Weckhuysen S., Frangu M., Neubauer B. A., Uldall P., Striano P., Zara F., Kleiss R., Simpson M., Muhle H., Nikanorova M., Jepsen B., Tommerup N., Stephani U., Guerrini R., Duno M., Hjalgrim H., Pal D., Helbig I. & Møller R. S. (20160408). The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. : Epilepsia.
Chicago
Larsen Jan, Johannesen Katrine Marie, Ek Jakob, Tang Shan, Marini Carla, Blichfeldt Susanne, Kibaek Maria, von Spiczak Sarah, Weckhuysen Sarah, Frangu Mimoza, Neubauer Bernd Axel, Uldall Peter, Striano Pasquale, Zara Federico, Kleiss Rebecca, Simpson Michael, Muhle Hiltrud, Nikanorova Marina, Jepsen Birgit, Tommerup Niels, Stephani Ulrich, Guerrini Renzo, Duno Morten, Hjalgrim Helle, Pal Deb, Helbig Ingo and Møller Rikke Steensbjerre. 20160408. The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. : Epilepsia.
Harvard
Larsen J., Johannesen K. M., Ek J., Tang S., Marini C., Blichfeldt S., Kibaek M., von Spiczak S., Weckhuysen S., Frangu M., Neubauer B. A., Uldall P., Striano P., Zara F., Kleiss R., Simpson M., Muhle H., Nikanorova M., Jepsen B., Tommerup N., Stephani U., Guerrini R., Duno M., Hjalgrim H., Pal D., Helbig I. and Møller R. S. (20160408). The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. : Epilepsia.
MLA
Larsen Jan, Johannesen Katrine Marie, Ek Jakob, Tang Shan, Marini Carla, Blichfeldt Susanne, Kibaek Maria, von Spiczak Sarah, Weckhuysen Sarah, Frangu Mimoza, Neubauer Bernd Axel, Uldall Peter, Striano Pasquale, Zara Federico, Kleiss Rebecca, Simpson Michael, Muhle Hiltrud, Nikanorova Marina, Jepsen Birgit, Tommerup Niels, Stephani Ulrich, Guerrini Renzo, Duno Morten, Hjalgrim Helle, Pal Deb, Helbig Ingo and Møller Rikke Steensbjerre. The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. : Epilepsia. 20160408.