Autosomal recessive cerebellar ataxia: A clinical and genetic study

Autosomal recessive cerebellar ataxia: A clinical and genetic study. L. Ali-Pacha, W. Hamza, S. Nouioua, C. Lagier-Tourenne, S. Assami, T. Benhassine, M. Koenig, M. Tazir. Journal of the Neurological Sciences, Volume 333, Supplement 1, 15 October 2013, Page e468. http://dx.doi.org/10.1016/j.jns.2013.07.1665

Friedreich's ataxia was the most frequent entity, as found in the majority of studies, followed by AOA2 and AVED.