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脊髓小脑性共济失调一例

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作者 杨俊峰
出处 《内蒙古医学杂志》 2009年第12期1521-1521,共1页 Inner Mongolia Medical Journal
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  • 1Went L. Guildlines for the molecular genetic predictive testing in Huntington's disease. J Med Genet, 1994,31:555-559
  • 2Margolis RL. The spinocerebellar ataxias:orders emerges from chaos. Curr Neurol Neurosci Rep, 2002,2:447-456
  • 3Mahowald WB, Verp MS, Anderson RR. GENETIC COUNSELING: clinical and ethical challenges. Annu Rev Genet, 1998, 32:547-559
  • 4Kirkwood SC, Siemers E, Bood C, et al.Confirmation of subtle motor changes among presymptomatic carriers of the Huntigton disease gene. Arch Neurol, 2000,57(7):1040-1044
  • 5Tan EK, Ashizawa T. Genetic testing in spinocerebellar ataxias: defining a clinical role. Arch Neurol, 2001,58(2):191-195
  • 6Harding AE. Clinical features and classification of inherited ataxias. Adv Neurol, 1993,61:1-14
  • 7Kawaguchi Y, Okamoto T, Taniwaki, et al. CAG expansion in a novel gene for Machado-Joseph disease at chromosome 14q 32.1. Nat Genet, 1994, 8:221-228
  • 8Pulst SM, Nechiporuk T, et al. Moderate expansion of a normary bialletic trinucleotide repeat in spinocerebellar ataxia type 2 gene on human chromosome 12. Nat Genet 1996,14:269-276
  • 9Orr H, Chung MY, Banfi S, et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet, 1993,4:221-226
  • 10Zhuchenko O, Bailey J, Bonnen P, et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small ployglutamine expansion in the alpha 1A-voltage-dependent calcium channel. Nat Genet, 1997,15:62-69

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