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