Mitochondrial Dysfunction in Spinocerebellar Ataxia Type 3 Is Linked to VDAC1 Deubiquitination
Tina Harmuth(University of Tübingen), Jeannette Hübener‐Schmid(Universitätsklinikum Tübingen), Julia C. Fitzgerald(Nottingham Trent University), Anna Sowa(University of Hohenheim), Jana Schmidt(University of Tübingen), Lüdger Schöls(German Center for Neurodegenerative Diseases), Anna J. Zimmer(University of Tübingen), Olaf Riess(University of Tübingen), Jonasz Jeremiasz Weber(University Hospitals of the Ruhr-University of Bochum)
Cited by 25
Related Papers
Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7
|Progress in Neurobiology|2013|360
Deep Intronic <i>FGF14</i> GAA Repeat Expansion in Late-Onset Cerebellar Ataxia
|New England Journal of Medicine|2022|243
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum
|Orphanet Journal of Rare Diseases|2013|189