- Pulst, S.M. and Perlman, S.L.. Hereditary ataxias in "Neurogenetics" (Pulst, S.M., ed.). Oxford University Press, New York, 2000. Pp. 231-264.
- Harding, A.E., Clinical features and classification of inherited ataxias. Advances in Neurology 1993; 61:1-14.
- Koide, R. et al, A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? Human Molecular Genetics 1999; 8:2047-2053.
- Fujigasaki, H. et al, CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia. Brain 2001; 124:1939-1947.
- Nakamura, K. et al, SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein. Human Molecular Genetics 2001; 10:1441-1448.
- Zühlke, C. et al, 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; 9:160-164.
- Kao, C.C. et al, Cloning of a transcriptionally active human TATA binding factor. Science 1990; 248:1646-1650.
- Pulst, S.M., Ataxia Overview in "Genetics of Movement Disorders" (Pulst, S.M., ed.); Academic Press, San Diego, 2003.
