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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2012 | 1 |
2013 | 1 |
2024 | 0 |
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Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.
Orphanet J Rare Dis. 2013 Jan 18;8:14. doi: 10.1186/1750-1172-8-14.
Orphanet J Rare Dis. 2013.
PMID: 23331413
Free PMC article.
Review.
Polymorphic genes of detoxification and mitochondrial enzymes and risk for progressive supranuclear palsy: a case control study.
Potts LF, Cambon AC, Ross OA, Rademakers R, Dickson DW, Uitti RJ, Wszolek ZK, Rai SN, Farrer MJ, Hein DW, Litvan I.
Potts LF, et al.
BMC Med Genet. 2012 Mar 17;13:16. doi: 10.1186/1471-2350-13-16.
BMC Med Genet. 2012.
PMID: 22424094
Free PMC article.
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Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.
Whaley NR, Fujioka S, Wszolek ZK.
Whaley NR, et al.
Orphanet J Rare Dis. 2011 May 28;6:33. doi: 10.1186/1750-1172-6-33.
Orphanet J Rare Dis. 2011.
PMID: 21619691
Free PMC article.
Review.
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