Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development

标题
Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development
作者
关键词
-
出版物
Disease Models & Mechanisms
Volume 5, Issue 6, Pages 921-929
出版商
The Company of Biologists
发表日期
2012-06-27
DOI
10.1242/dmm.010157

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