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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Mov Disord Clin Pract
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley & Sons, Inc. 2020
Konular:
Research Articles
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller