Brain atrophy measures in preclinical and manifest spinocerebellar ataxia type 2.
Kathrin ReetzRoberto Rodríguez-LabradaImis DoganShahram MirzazadeSandro RomanzettiJörg B SchulzEdilia M Cruz-RivasJose A Alvarez-CuestaRaul Aguilera RodríguezYanetza Gonzalez ZaldivarGeorg AuburgerLuis Velázquez-PérezPublished in: Annals of clinical and translational neurology (2018)
Preclinical SCA2 mutation carriers exhibit brain abnormalities, which could be targeted as surrogate parameters for disease progression and in future preventive trials.