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Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development |
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| Authors: | Fadi A. Issa Allan F. Mock Alvaro Sagasti Diane M. Papazian |
| Affiliation: | 1.Department of Physiology;2.Department of Molecular, Cell and Developmental Biology;3.Brain Research Institute;4.Molecular Biology Institute, and;5.David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095-1751, USA |
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