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Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy

Document Type

Article

Author

Gauquelin, L.; Ahmed, S.; Yoon, G.; Hartley, T.; Dyment, D.A.; Geraghty, M.T.; Rojas, S.; Boycott, K.M.; Tarnopolsky, M.; Brais, B.; Choquet, K.; Rouleau, G.; Tétreault, M.; Majewski, J.; Bernier, F.; Innes, A.M.; Suchowersky, O.

Source

In: Movement Disorders Clinical Practice. (Movement Disorders Clinical Practice, 1 November 2020, 7(8):940-949)

Subject

Language

English

ISSN

23301619

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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