Publications by authors named "Sandrine Correia"
Background: Spinocerebellar ataxia type 21 (SCA21) is a rare inherited neurological disorder characterized by motor, cognitive, and behavioral disturbances, caused by autosomal dominant TMEM240 variants.
Objectives: To identify the genetic cause of a dystonic tremor with autosomal dominant inheritance.
Methods: Six subjects of a multi-generational French family affected by tremor and dystonia were studied.