Leiden University Scholarly Publications

Your Search

Enabled Filters

  • (-) = Lohmann, E.

Refine Results

Resource Type

Availability

Faculty

Collection

Author

Language

Search results

  • RSS Feed
(1 - 2 of 2)
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
metadata only
A Correction to this paper has been published: https://doi.org/10.1038/s41436-020-01064-y
Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Lesage, S.; Drouet, V.; Majounie, E.; Deramecourt, V.; Jacoupy, M.; Nicolas, A.; ... ; IPDGC 2016
Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Article / Letter to editor
metadata only