Abnormal eyeblink conditioning is an early marker of cerebellar dysfunction in preclinical SCA3 mutation carriers

BACKGROUND: Spinocerebellar ataxias (SCAs) are a group of autosomal dominantly inherited degenerative diseases. As the pathological process probably commences years before the first appearance of clinical symptoms, preclinical carriers of a SCA mutation offer the opportunity to study the earliest st...

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Detalles Bibliográficos
Autores principales: van Gaalen, J., Maas, R. P. P. W. M., Ippel, E. F., Elting, M. W., van Spaendonck-Zwarts, K. Y., Vermeer, S., Verschuuren-Bemelmans, C., Timmann, D., van de Warrenburg, Bart P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373441/
https://www.ncbi.nlm.nih.gov/pubmed/30430184
http://dx.doi.org/10.1007/s00221-018-5424-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373441/
https://www.ncbi.nlm.nih.gov/pubmed/30430184
http://dx.doi.org/10.1007/s00221-018-5424-y

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