Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca21 channel gene CACNL1A4.
Authors: Ophoff et al.
Share this article
Sign Up For An MSC Newsletter
Sign Up for MSC Content Alerts!
Interested in receiving notifications about new MSC content? Then sign up for our content alerts and be the first to know about our latest articles, literature recaps and more!