CareLit · DOI-Nachweis · Aktuelle Neurologie
Glucose transporter 1 gene mutations cause sporadic PED
DOI 10.1055/s-0029-1238859
Bibliografische Angaben
Nachweis in CareLit
Autor:innenS Schneider, C Paisan-Ruiz, I Garcia-Gorostiaga, NP Quinn, YG Weber, H Lerche, J Hardy, K Bhatia
ZeitschriftAktuelle Neurologie
Ausgabe10/2009
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background: Paroxysmal exercise-induced dyskinesias (PED) are involuntary intermittent movements triggered by prolonged physical exertion. Autosomal dominant inheritance may occur. Recently, mutations in the glucose transporter 1 (GLUT1) gene (chr. 1p35-p31.3) have been identified as a cause in some patients with autosomal dominant PED. Mutations in this gene have previously been associated with the GLUT1 deficiency…
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Zitierempfehlung
S Schneider, C Paisan-Ruiz, I Garcia-Gorostiaga, NP Quinn, YG Weber, H Lerche, J Hardy, K Bhatia (2009) Glucose transporter 1 gene mutations cause sporadic PED. Aktuelle Neurologie (10). https://doi.org/10.1055/s-0029-1238859
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