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Volumn 8, Issue 2, 2009, Pages 104-107

Spinocerebellar ataxia type 23: A Genetic update

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

EID: 67949115850     PISSN: 14734222     EISSN: 14734230     Source Type: Journal    
DOI: 10.1007/s12311-008-0085-1     Document Type: Article
Times cited : (16)

References (17)
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  • 2
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  • 3
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    • Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus
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  • 7
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    • Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis
    • C Mariotti A Brusco D Di Bella C Cagnoli M Seri C Gellera 2008 Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis Cerebellum 7 2 184 188
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  • 8
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    • A duplication at chromosome 11q12.2-11q12.3 is associated with Spinocerebellar Ataxia Type 20 (SCA20)
    • doi: 10.1093/hmg/ddn283
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    • (2008) Hum Mol Genet
    • Knight, M.A.1    Hernandez, D.2    Diede, S.J.3    Dauwerse, H.G.4    Rafferty, I.5    Van De Leemput, J.6
  • 11
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    • Autosomal dominant cerebellar ataxias: Clinical features, genetics, and pathogenesis
    • DOI 10.1016/S1474-4422(04)00737-9, PII S1474442204007379
    • L Schols P Bauer T Schmidt T Schulte O Riess 2004 Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis Lancet Neurol 3 5 291 304 (Pubitemid 38510200)
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  • 13
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    • DOI 10.1007/s004390051026
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.