Browse by Journal Title

2018

Dominant SCN2A mutation causes familial episodic ataxia and impairment of speech development.
Fazeli, W. and Becker, K. and Herkenrath, P. and Düchting, C. and Körber, F. and Landgraf, P. and Nürnberg, P. and Altmüller, J. and Thiele, H. and Koy, A. and Liebau, M.C. and Simon, T. and Dötsch, J. and Cirak, S.
Neuropediatrics 49 (6): 379-384. December 2018