Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development
Issa, F. A., Mock, A. F., Sagasti, A., Papazian, D. M.Volume:
5
Language:
english
Journal:
Disease Models & Mechanisms
DOI:
10.1242/dmm.010157
Date:
November, 2012
File:
PDF, 1.88 MB
english, 2012