The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia

OBJECTIVES—To investigate if sequence alterations of the excitatory amino acid transporter gene EAAT2 (GLT-1) may be a contributory factor to the pathogenesis of motor system degeneration. EAAT2 serves as a candidate gene as its reduced expression was reported in patients with amyotrophic lateral sc...

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Bibliographic Details
Main Authors: Meyer, T., Munch, C., Volkel, H., Booms, P., Ludolph, A.
Format: Artigo
Language:Inglês
Published: BMJ Group 1998
Subjects:
Short Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2170294/
https://ncbi.nlm.nih.gov/pubmed/9771796
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