DOI:
10.1055/s-00000071
Seminars in Neurology
LinksClose Window
References
Kaunisto MA, Harno H, Vanmolkot KR. et al.
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2
Neurogenetics 2004; 5: 141-146
Search in:
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.