Paroxysmal Exercise-induced Dyskinesias Caused by GLUT1 Deficiency Syndrome

BACKGROUND: Glucose transporter type 1 deficiency syndrome is due to de novo mutations in the SLC2A1 gene encoding the glucose transporter type 1. PHENOMENOLOGY SHOWN: Paroxysmal motor manifestations induced by exercise or fasting may be the main manifestations of glucose transporter type 1 deficien...

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Detalles Bibliográficos
Autores principales: Mongin, Marie, Mezouar, Nicolas, Dodet, Pauline, Vidailhet, Marie, Roze, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Columbia University Libraries/Information Services 2016
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Video Abstracts
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4790204/
https://www.ncbi.nlm.nih.gov/pubmed/27351150
http://dx.doi.org/10.7916/D89W0F96

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4790204/
https://www.ncbi.nlm.nih.gov/pubmed/27351150
http://dx.doi.org/10.7916/D89W0F96

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