Published in
Elsevier, Genetics in Medicine, 10(23), p. 2021, 2021
DOI: 10.1038/s41436-020-01064-y
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Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment
Journal article published in 2021 by
Thomas Roux 
,
Mathieu Barbier,
Mélanie Papin,
Claire-Sophie Davoine,
Sabrina Sayah,
Giulia Coarelli,
Perrine Charles,
Cecilia Marelli,
Livia Parodi,
Christine Tranchant,
Cyril Goizet,
Stephan Klebe,
Ebba Lohmann,
Lionel Van Maldergem,
Christine van Broeckhoven
and other authors.
,
Mathieu Barbier,
Mélanie Papin,
Claire-Sophie Davoine,
Sabrina Sayah,
Giulia Coarelli,
Perrine Charles,
Cecilia Marelli,
Livia Parodi,
Christine Tranchant,
Cyril Goizet,
Stephan Klebe,
Ebba Lohmann,
Lionel Van Maldergem,
Christine van Broeckhoven
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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