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![Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (vol 22, pg 1851, 2020)](https://scholarlypublications.universiteitleiden.nl/sites/all/themes/scholarly/img/closed_access.png)
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (vol 22, pg 1851, 2020)
- All authors
- Roux, T.; Barbier, M.; Papin, M.; Davoine, C.S.; Sayah, S.; Coarelli, G.; Charles, P.; Marelli, C.; Parodi, L.; Tranchant, C.; Goizet, C.; Klebe, S.; Lohmann, E.; Maldergem, L. van; Broeckhoven, C. van; Coutelier, M.; Tesson, C.; Stevanin, G.; Duyckaerts, C.; Brice, A.; Durr, A.; SPATAX Network
- Date
- 2020-12-22
- Journal
- Genetics in Medicine