Paper
Paper
Search...
Search ResearchHub...
Ctrl+K
New
Home
Browse
Earn
Fund
RH Journal
Notebook
Lists
Leaderboard
RSC
USD
Changelog
Terms
Privacy
Issues
Docs
Support
Foundation
About
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 A... | ResearchHub
Paper
Paper
Search...
Search ResearchHub...
Ctrl+K
New
Home
Browse
Earn
Fund
RH Journal
Notebook
Lists
Leaderboard
RSC
USD
Changelog
Terms
Privacy
Issues
Docs
Support
Foundation
About
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
0
Authors
Roel Ophoff
24 more
Roel Ophoff
•
Gisela Terwindt
22 more
•
Rune Frants
Published
November 1, 1996
Paper
Conversation
0
Reviews
0
Bounties
0
Sign in to review
Share your thoughts on this paper...
Best
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Cell
Topics
Biology
Neuroscience
Medicine
Internal Medicine
Neurology
Show all topics
DOI
10.1016/s0092-8674(00)81373-2
License
publisher-specific-oa
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Cell
Topics
Biology
Neuroscience
Medicine
Internal Medicine
Neurology
Show all topics
DOI
10.1016/s0092-8674(00)81373-2
License
publisher-specific-oa
