Issa, F. A., Mock, A. F., Sagasti, A., & Papazian, D. M. (2012). Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development. The Company of Biologists Limited.
Citação norma ChicagoIssa, Fadi A., Allan F. Mock, Alvaro Sagasti, and Diane M. Papazian. Spinocerebellar Ataxia Type 13 Mutation That Is Associated With Disease Onset in Infancy Disrupts Axonal Pathfinding During Neuronal Development. The Company of Biologists Limited, 2012.
MLA CitationIssa, Fadi A., Allan F. Mock, Alvaro Sagasti, and Diane M. Papazian. Spinocerebellar Ataxia Type 13 Mutation That Is Associated With Disease Onset in Infancy Disrupts Axonal Pathfinding During Neuronal Development. The Company of Biologists Limited, 2012.