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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
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  1. Professor Albert C Ludolph, University of Ulm, Department of Neurology, Steinhövelstrasse 9, 89081 Ulm, Germany. Telephone 0049 731 177 1200; fax 0049 731 177 1202.
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Citation

Meyer T, Münch C, Völkel H, et al
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

Publication history

  • Received September 5, 1997
  • Revised January 26, 1998
  • Accepted March 19, 1998
  • First published October 1, 1998.
Online issue publication 
October 01, 1998

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