CareLit · DOI-Nachweis · Klinische Neurophysiologie
Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA 17)
DOI 10.1055/s-2006-939170
Bibliografische Angaben
Nachweis in CareLit
Autor:innenJ Hübner, A Sprenger, J Hagenah, C Klein, H Rambold, C Zühlke, D Kömpf, A Rolfs, H Kimmig, C Helmchen
ZeitschriftKlinische Neurophysiologie
Ausgabe03/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
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 compa…
Zitieren
Zitierempfehlung
J Hübner, A Sprenger, J Hagenah, C Klein, H Rambold, C Zühlke, D Kömpf, A Rolfs, H Kimmig, C Helmchen (2006) Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA 17). Klinische Neurophysiologie (03). https://doi.org/10.1055/s-2006-939170
Mit CareLit weiterarbeiten