CTA/CTG expansions at the SCA 8 locus in multiple system atrophy

[1]  H. Ito,et al.  Clinicopathologic investigation of a family with expanded SCA8 CTA/CTG repeats , 2006, Neurology.

[2]  Harry T Orr,et al.  Targeted Deletion of a Single Sca8 Ataxia Locus Allele in Mice Causes Abnormal Gait, Progressive Loss of Motor Coordination, and Purkinje Cell Dendritic Deficits , 2006, The Journal of Neuroscience.

[3]  M. Farrer,et al.  Sporadic SCA8 mutation resembling corticobasal degeneration. , 2005, Parkinsonism & related disorders.

[4]  S. Factor,et al.  False‐positive SCA8 gene test in a patient with pathologically proven multiple system atrophy , 2005, Annals of neurology.

[5]  A. Zeman,et al.  Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports , 2004, Journal of Neurology, Neurosurgery & Psychiatry.

[6]  D. Hoffman-Zacharska,et al.  SCA8 repeat expansion coexists with SCA1--not only with SCA6. , 2003, American journal of human genetics.

[7]  H. Topka,et al.  Do CTG expansions at the SCA8 locus cause ataxia? , 2003, Annals of neurology.

[8]  M. Oda,et al.  SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6. , 2003, American journal of human genetics.

[9]  M. Savontaus,et al.  Calculating predictive values for the large repeat alleles at the SCA8 locus in patients with ataxia , 2002, Journal of medical genetics.

[10]  S. Sorbi,et al.  Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy. , 2001, Archives of neurology.

[11]  D. Geschwind,et al.  SCA8 repeat expansions in ataxia: A controversial association , 2001, Neurology.

[12]  L. Schut,et al.  Spinocerebellar ataxia type 8 , 2000, Neurology.

[13]  T. Bird,et al.  SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance. , 2000, Human molecular genetics.

[14]  L. Schöls,et al.  Genetic background of apparently idiopathic sporadic cerebellar ataxia , 2000, Human Genetics.

[15]  Y. Agid,et al.  Are (CTG)n expansions at the SCA8 locus rare polymorphisms? , 2000, Nature Genetics.

[16]  P. Maciel,et al.  High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles. , 2000, American journal of human genetics.

[17]  T. Bird,et al.  An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8) , 1999, Nature Genetics.

[18]  J. Jankovic,et al.  Consensus statement on the definition of orthostatic hypotension, pure autonomic failure and multiple system atrophy , 2005, Clinical Autonomic Research.

[19]  N. Wood,et al.  Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia , 2000, Nature Genetics.