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

BACKGROUND: Cerebellar atrophy is a nonspecific imaging finding observed in a number of neurological disorders. Genetic ataxias associated with cerebellar atrophy are a heterogeneous group of conditions, rendering the approach to diagnosis challenging. OBJECTIVES: To define the spectrum of genetic a...

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Bibliografische gegevens
Gepubliceerd in:Mov Disord Clin Pract
Hoofdauteurs: Gauquelin, Laurence, Hartley, Taila, Tarnopolsky, Mark, Dyment, David A., Brais, Bernard, Geraghty, Michael T., Tétreault, Martine, Ahmed, Sohnee, Rojas, Samantha, Choquet, Karine, Majewski, Jacek, Bernier, François, Innes, Allan Micheil, Rouleau, Guy, Suchowersky, Oksana, Boycott, Kym M., Yoon, Grace
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: John Wiley & Sons, Inc. 2020
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Research Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7604675/
https://ncbi.nlm.nih.gov/pubmed/33163565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.13086
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