Group by:
Date |
Item TypeArticle
Dominant SCN2A mutation causes familial episodic ataxia and impairment of speech development.
Fazeli, W., Becker, K., Herkenrath, P., Düchting, C., Körber, F., Landgraf, P., Nürnberg, P., Altmüller, J.
ORCID: https://orcid.org/0000-0003-4372-1521, Thiele, H., Koy, A., Liebau, M.C., Simon, T., Dötsch, J. and Cirak, S.
Neuropediatrics 49
(6): 379-384.
December 2018
This list was generated on Sat Nov 14 05:59:07 2026 UTC.