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

Author(s):
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
Published
2020
Publication type
Article / Letter to editor

Abstract

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

Date issued
2020-12-22
Language
English
Publisher
SPRINGERNATURE
Is part of
Genetics in Medicine
hdl
1887/3184674
doi
10.1038/s41436-020-01064-y