Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds.

@article{Bauer2010SpinocerebellarAT,
  title={Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds.},
  author={Peter Bauer and Giovanni Stevanin and Christian Beetz and Matthis Synofzik and Tanja Schmitz-H{\"u}bsch and U. W{\"u}llner and Eric Berthier and Elisabeth Ollagnon-Roman and Olaf Riess and Sylvie Forlani and Emeline Mundwiller and Alexandra Durr and Ludger Sch{\"o}ls and Alexis Brice},
  journal={Journal of neurology, neurosurgery, and psychiatry},
  year={2010},
  volume={81 11},
  pages={1229-32}
}
BACKGROUND At least 28 loci have been linked to autosomal dominant spinocerebellar ataxia (ADCA). Causative genes have been cloned for 10 nucleotide repeat expansions (SCA1, 2, 3, 6, 7, 8, 10, 12, 17 and 31) and six genes with classical mutations (SCA5, 13, 14, 15/16, 27 and 28). Recently, a large British pedigree linked to SCA11 has been reported to carry a mutation in the TTBK2 gene. In order to assess the prevalence and phenotypic spectrum of SCA11, the authors screened 148 index patients of… CONTINUE READING