Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment

MLA

Thomas Roux, et al. Clinical, Neuropathological, and Genetic Characterization of STUB1 Variants in Cerebellar Ataxias: A Frequent Cause of Predominant Cognitive Impairment. Nov. 2020. EBSCOhost, https://doi.org/10.1038/s41436-020-0899-x⟩.

APA

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, Marie Coutelier, Christelle Tesson, Giovanni Stevanin, Charles Duyckaerts, … Nicholas Wood. (2020). Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment. https://doi.org/10.1038/s41436-020-0899-x⟩

Chicago

Thomas Roux, Mathieu Barbier, Mélanie Papin, Claire-Sophie Davoine, Sabrina Sayah, Giulia Coarelli, Perrine Charles, et al. 2020. “Clinical, Neuropathological, and Genetic Characterization of STUB1 Variants in Cerebellar Ataxias: A Frequent Cause of Predominant Cognitive Impairment,” November. doi:10.1038/s41436-020-0899-x⟩.