De novo mutations in ATP1A2 and CACNA1A are frequent in...

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine

Riant, F., Ducros, A., Ploton, C., Barbance, C., Depienne, C., Tournier-Lasserve, E.
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
75
Language:
english
Journal:
Neurology
DOI:
10.1212/wnl.0b013e3181f25e8f
Date:
September, 2010
File:
PDF, 277 KB
english, 2010
Conversion to is in progress
Conversion to is failed