![](/img/cover-not-exists.png)
Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine
Kinder, S., Ossig, C., Wienecke, M., Beyer, A., von der Hagen, M., Storch, A., Smitka, M.Volume:
19
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/j.ejpn.2014.10.005
Date:
January, 2015
File:
PDF, 649 KB
english, 2015