APA
Krabichler B., Rostasy K., Baumann M., Karall D., Scholl-Bürgi S., Schwarzer C., Gautsch K., Spreiz A., Kotzot D., Zschocke J., Fauth C. & Haberlandt E. (20120822). Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy. : Annals of human genetics.
Chicago
Krabichler Birgit, Rostasy Kevin, Baumann Matthias, Karall Daniela, Scholl-Bürgi Sabine, Schwarzer Christoph, Gautsch Kurt, Spreiz Ana, Kotzot Dieter, Zschocke Johannes, Fauth Christine and Haberlandt Edda. 20120822. Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy. : Annals of human genetics.
Harvard
Krabichler B., Rostasy K., Baumann M., Karall D., Scholl-Bürgi S., Schwarzer C., Gautsch K., Spreiz A., Kotzot D., Zschocke J., Fauth C. and Haberlandt E. (20120822). Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy. : Annals of human genetics.
MLA
Krabichler Birgit, Rostasy Kevin, Baumann Matthias, Karall Daniela, Scholl-Bürgi Sabine, Schwarzer Christoph, Gautsch Kurt, Spreiz Ana, Kotzot Dieter, Zschocke Johannes, Fauth Christine and Haberlandt Edda. Novel mutation in potassium channel related gene KCTD7 and progressive myoclonic epilepsy. : Annals of human genetics. 20120822.