CareLit · DOI-Nachweis · Aktuelle Neurologie
Saccadic eye movement deficits in PINK1 mutation carriers
DOI 10.1055/s-2006-953055
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Autor:innenS. Hertel, A. Sprenger, D. Kömpf, C. Klein, C. Helmchen, H. Kimmig
ZeitschriftAktuelle Neurologie
Ausgabe09/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Introduction: Saccadic eye movement abnormalities often occur in patients with parkinsonian syndromes. Recessively inherited mutations in the recently identified PINK1 gene cause familial parkinsonism; PINK1 mutation carriers may represent individuals at risk who can be identified prior to the development of symptoms by molecular genetic testing. We searched for dysfunctions of saccadic eye movements in clinically u…
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Zitierempfehlung
S. Hertel, A. Sprenger, D. Kömpf, C. Klein, C. Helmchen, H. Kimmig (2006) Saccadic eye movement deficits in PINK1 mutation carriers. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2006-953055
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