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23. The relationship between (CAG)n repeat number and age of onset in a family with dentatorubral-pallidoluysian atrophy (DRPLA): diagnostic implications of confirmatory and predictive testing. Potter NT J Med Genet; 1996 Feb; 33(2):168-70. PubMed ID: 8929958 [TBL] [Abstract][Full Text] [Related]
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28. Homozygosity for an allele carrying intermediate CAG repeats in the dentatorubral-pallidoluysian atrophy (DRPLA) gene results in spastic paraplegia. Kurohara K; Kuroda Y; Maruyama H; Kawakami H; Yukitake M; Matsui M; Nakamura S Neurology; 1997 Apr; 48(4):1087-90. PubMed ID: 9109905 [TBL] [Abstract][Full Text] [Related]
29. Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p. Nagafuchi S; Yanagisawa H; Sato K; Shirayama T; Ohsaki E; Bundo M; Takeda T; Tadokoro K; Kondo I; Murayama N Nat Genet; 1994 Jan; 6(1):14-8. PubMed ID: 8136826 [TBL] [Abstract][Full Text] [Related]
30. DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation. Komure O; Sano A; Nishino N; Yamauchi N; Ueno S; Kondoh K; Sano N; Takahashi M; Murayama N; Kondo I Neurology; 1995 Jan; 45(1):143-9. PubMed ID: 7824105 [TBL] [Abstract][Full Text] [Related]
31. The relationship between the number of CAG repeats and clinical manifestations: a survey of Chinese DRPLA family. Sun S; Zhao W; Liu X Acta Neurol Belg; 2023 Aug; 123(4):1505-1510. PubMed ID: 37243799 [TBL] [Abstract][Full Text] [Related]
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39. Dentatorubral-pallidoluysian atrophy in three generations, with clinical courses from nearly asymptomatic elderly to severe juvenile, in an Australian family of Macedonian descent. Vinton A; Fahey MC; O'Brien TJ; Shaw J; Storey E; Gardner RJ; Mitchell PJ; Du Sart D; King JO Am J Med Genet A; 2005 Jul; 136(2):201-4. PubMed ID: 15948186 [TBL] [Abstract][Full Text] [Related]
40. Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1. Hashida H; Goto J; Kurisaki H; Mizusawa H; Kanazawa I Ann Neurol; 1997 Apr; 41(4):505-11. PubMed ID: 9124808 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]