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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)
Roux, T.; Barbier, M.; Papin, M.; Davoine, C.S.; Sayah, S.; Coarelli, G.; ... ; SPATAX Network 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (vol 22, pg 1851, 2020)
Article / Letter to editor
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A Correction to this paper has been published: https://doi.org/10.1038/s41436-020-01064-y
Mutation (variation) databases and registries: a rationale for coordination of efforts
Auerbach, A.D.; Burn, J.; Cassiman, J.J.; Claustres, M.; Cotton, R.G.H.; Cutting, G.; ... ; Human Variome Project 2011
Mutation (variation) databases and registries: a rationale for coordination of efforts
Article / Letter to editor
metadata only