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

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Bibliographic Details
Title: Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development.
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
Description
ISSN:1754-8411
DOI:10.1242/dmm.010157