Published in
Elsevier, Genetics in Medicine, 6(23), p. 1171-1172, 2021
DOI: 10.1038/s41436-021-01104-1
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Correspondence on “Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment” by Roux et al.
Journal article published in 2021 by
Joohyun Park,
Natalie Deininger,
Maren Rautenberg,
Carsten Saft,
Florian Harmuth,
Marc Sturm 
,
Olaf Riess,
Ludger Schöls,
Matthis Synofzik,
Tobias B. Haack
,
Olaf Riess,
Ludger Schöls,
Matthis Synofzik,
Tobias B. Haack
This paper is made freely available by the publisher.
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