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A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking.
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- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0173565
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- Article
Mutant β-III Spectrin Causes mGluR1α Mislocalization and Functional Deficits in a Mouse Model of Spinocerebellar Ataxia Type 5.
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- Journal of Neuroscience, 2014, v. 34, n. 30, p. 9891, doi. 10.1523/JNEUROSCI.0876-14.2014
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- Article