Behavioral Disorder, Dementia, Ataxia, and Rigidity in a Large Family With TATA Box-Binding Protein Mutation

This publication has 19 references indexed in Scilit:

• SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
  Human Molecular Genetics, 2001
• Executive Dysfunction in Spinocerebellar Ataxia Type 1
  European Neurology, 2001
• Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia
  European Journal of Human Genetics, 2001
• SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion
  Neurology, 2001
• Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG Trinucleotide Repeat Expansion in Patients With Hereditary Spinocerebellar Ataxia From Chinese Kindreds
  Archives of Neurology, 2000
• A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? [In Process Citation]
  Human Molecular Genetics, 1999
• The Gene for the TATA Binding Protein (TBP) That Contains a Highly Polymorphic Protein Coding CAG Repeat Maps to 6q27
  Genomics, 1994
• Functional Domains and Upstream Activation Properties of Cloned Human TATA Binding Protein
  Science, 1990
• Cloning of a Transcriptionally Active Human TATA Binding Factor
  Science, 1990
• Unusual form of cerebellar ataxia
  Neurology, 1958