Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (vol 22, pg 1851, 2020)

Roux, T.; Barbier, M.; Papin, M.; Davoine, C.S.; Sayah, S.; Coarelli, G.; ... ; SPATAX Network (2020)

Article / Letter to editor

A Correction to this paper has been published: https://doi.org/10.1038/s41436-020-01064-y

• 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
• DOI: doi:10.1038/s41436-020-01064-y