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

Publikation auf PubMed: https://pubmed.ncbi.nlm.nih.gov/9771796
Publikation im Volltext: https://jnnp.bmj.com/content/65/4/594.long