Authors
Coutelier M., Burglen L., Mundwiller E. ...Durr A.
Journal
Neurology,
Publication date
April 2015
Abstract
In a large family of Algerian origin, we aimed to identify the genetic mutation segregating with simultaneous presence of adult-onset, paucisymptomatic, slowly progressive, cerebellar ataxia in 7 adults and congenital ataxia in 1 child, and then to assess the involvement of GRID2 mutations in 144 patients with congenital cerebellar ataxia.
DOI link
10.1212/WNL.0000000000001524
