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Year | Number of Results |
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2005 | 1 |
2009 | 1 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
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Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin.
Hum Mol Genet. 2009 Oct 1;18(19):3533-43. doi: 10.1093/hmg/ddp298. Epub 2009 Jun 26.
Hum Mol Genet. 2009.
PMID: 19561170
SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG gene.
Koht J, Stevanin G, Durr A, Mundwiller E, Brice A, Tallaksen CM.
Koht J, et al.
Acta Neurol Scand. 2012 Feb;125(2):116-22. doi: 10.1111/j.1600-0404.2011.01504.x. Epub 2011 Mar 21.
Acta Neurol Scand. 2012.
PMID: 21434874
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The clinical and genetic spectrum of spinocerebellar ataxia 14.
Chen DH, Cimino PJ, Ranum LP, Zoghbi HY, Yabe I, Schut L, Margolis RL, Lipe HP, Feleke A, Matsushita M, Wolff J, Morgan C, Lau D, Fernandez M, Sasaki H, Raskind WH, Bird TD.
Chen DH, et al.
Neurology. 2005 Apr 12;64(7):1258-60. doi: 10.1212/01.WNL.0000156801.64549.6B.
Neurology. 2005.
PMID: 15824357
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