Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.

Authors: Ophoff et al.

Posted in Papers / Classic Papers / 

Cell. 1996 Nov 1;87(3):543-52.

PMID: 8898206 | DOI: 10.1016/s0092-8674(00)81373-2

Sign Up For An MSC Newsletter

Sign up for:

Register to Watch the MSC Emerging Science Contest!

The MSC Emerging Science Contest for Young Investigators will take place on Wednesday, December 13, 2023, from 8-10 PM Eastern (US) time. We welcome those who wish to watch the event as an attendee. Register here to attend, and learn more about the contest here.

Discussion

Leave a Comment

You must be logged in to post a comment.

Search

  • Content Types

  • Paper Categories

  • Paper Dates

Paper Categories

By Date