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?

Meyer T, Münch C, Völkel H, Booms P, Ludolph AC.
J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):594-6. doi: 10.1136/jnnp.65.4.594.
PMID: 9771796

Journal of Neurology, Neurosurgery and Psychiatry, Oktober 1998