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Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA 17)

J Hübner, A Sprenger, J Hagenah, C Klein, H Rambold, C Zühlke, D Kömpf, A Rolfs, H Kimmig, C Helmchen · Klinische Neurophysiologie · 2006 · Heft 03

Dokument
805077
CareLit-ID
Jahr
2006
Publikation
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Klinische Neurophysiologie
Autor:innen
J Hübner, A Sprenger, J Hagenah, C Klein, H Rambold, C Zühlke, D Kömpf, A Rolfs, H Kimmig, C Helmchen
Ausgabe
Heft 03 / 2006
Seiten
–
Erschienen: 2006-03-24 00:00:00
ISSN
1434-0275
DOI
10.1055/s-2006-939170

Zusammenfassung

Background: Spinocerebellar ataxia type 17 (SCA17) is associated with an expansion of CAG/CAA trinucleotide repeats in the gene encoding TATA-binding protein (TBP). The aim of this study was to characterize eye movements in SCA17 and to localize oculomotor deficits. Methods: Eye movements of 13 SCA17 mutation carriers and 13 age-matched control subjects were recorded using the video-based EYELINK II system and compared using ANOVA (p

Schlagworte

Klinische Neurophysiologie