Correspondence on "Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment" by Roux et al

Genet Med. 2021 Jun;23(6):1171-1172. doi: 10.1038/s41436-021-01104-1. Epub 2021 Feb 9.

Joohyun Park¹, Natalie Deininger², Maren Rautenberg², Carsten Saft³, Florian Harmuth², Marc Sturm², Olaf Riess^{2

4}, Ludger Schöls^{4

5

6}, Matthis Synofzik^{5

6}, Tobias B Haack^{2

4}

¹ Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. [email protected].
² Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
³ Department of Neurology, Huntington Centre NRW, Ruhr-University Bochum, St. Josef-Hospital, Bochum, Germany.
⁴ Centre for Rare Diseases, University of Tübingen, Tübingen, Germany.
⁵ Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
⁶ German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.

No abstract available

Publication types