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Miki T, Zwingman TA, Wakamori M, et al. 
Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies. [JOURNAL ARTICLE]
Neuroscience 2008 Jun 30.
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Xie G, Clapcote SJ, Nieman BJ, et al. 
Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A. [JOURNAL ARTICLE]
Genes Brain Behav 2007 Mar 21.
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Kaja S, Hann V, Payne HL, et al. 
Aberrant cerebellar granule cell-specific GABA(A) receptor expression in the epileptic and ataxic mouse mutant, Tottering. [JOURNAL ARTICLE]
Neuroscience 2007 Jul 4.
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Tonelli A, D'Angelo MG, Salati R, et al. 
Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. [Journal Article]
J Neurol Sci 2006 Feb 15; 241(1-2):13-7.
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Tokuda S, Kuramoto T, Tanaka K, et al. 
The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca(2+) channel alpha(1A) subunit gene and exhibits absence seizures. [JOURNAL ARTICLE]
Brain Res 2006 Dec 28.
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Etheredge JA, Murchison D, Abbott LC, et al. 
Functional compensation by other voltage-gated Ca(2+) channels in mouse basal forebrain neurons with Ca(V)2.1 mutations. [JOURNAL ARTICLE]
Brain Res 2005 Dec 16.
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Alonso I, Barros J, Tuna A, et al. 
Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family. [Journal Article]
Arch Neurol 2003 Apr; 60(4):610-4.
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Zwingman TA, Neumann PE, Noebels JL, et al. 
Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a. [Journal Article]
J Neurosci 2001 Feb 15; 21(4):1169-78.
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Pietrobon D 
Calcium channels and channelopathies of the central nervous system. [Journal Article, Review]
Mol Neurobiol 2002 Feb; 25(1):31-50.
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