Referenced in: none

Automatically associated channels: Cav2.1

Title: Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine.

Authors: S Kinder, C Ossig, M Wienecke, A Beyer, M von der Hagen, A Storch, M Smitka

Journal, date & volume: Eur. J. Paediatr. Neurol., 2015 Jan , 19, 72-4

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/25468264

Abstract