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 (Q41843474)
scientific article published on October 1, 1998
Language:
(P31) (Q13442814)
(P50) (Q67390363)
(Q92129179)
(P304) 594-596
(P407) (Q1860)
(P433) 4
(P478) 65
(P577) Thursday, October 1, 1998
Thursday, October 1, 1998
(P921) (Q206901)
(P953) https://jnnp.bmj.com/content/jnnp/65/4/594.full.pdf
https://europepmc.org/articles/PMC2170294
https://europepmc.org/articles/PMC2170294?pdf=render
https://syndication.highwire.org/content/doi/10.1136/jnnp.65.4.594
(P1433) (Q1599804)
(P1476) "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" (language: en)
(P2093) C. Münch
H. Völkel
P. Booms
other details
description scientific article published on October 1, 1998

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