Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development.
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| Title: | Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development. |
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| Authors: | Issa FA; Department of Physiology, University of California at Los Angeles, Los Angeles, CA 90095-1751, USA., Mock AF, Sagasti A, Papazian DM |
| Source: | Disease models & mechanisms [Dis Model Mech] 2012 Nov; Vol. 5 (6), pp. 921-9. Date of Electronic Publication: 2012 Jun 26. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Company of Biologists Ltd Country of Publication: England NLM ID: 101483332 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1754-8411 (Electronic) Linking ISSN: 17548403 NLM ISO Abbreviation: Dis Model Mech Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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