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CLINICAL

A novel p.E121G SOD1 mutation in slowly progressive form of amyotrophic lateral sclerosis induces cytoplasmic aggregates in cultured motor neurons and reduces cell viability

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Pages 131-134 | Received 30 Jun 2014, Accepted 09 Sep 2014, Published online: 22 Oct 2014

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Guillaume Taieb, Anne Polge, Raul Juntas-Morales, Nicolas Pageot, Serge Lumbroso, Kevin Mouzat & William Camu. (2017) Slowly progressive motor neuron disease with multi-system involvement related to p.E121G SOD1 mutation. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 18:3-4, pages 296-297.
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Cinzia Lucchesi, Elena Caldarazzo Ienco, Monica Fabbrini, Livia Pasquali, Annalisa Lo Gerfo, Antonella Fogli & Gabriele Siciliano. (2017) Amyotrophic lateral sclerosis with long lasting disease course and SOD1 and TARDBP mutations: Report of two cases and overview of the literature. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 18:1-2, pages 137-139.
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Articles from other publishers (2)

Shaherin Basith, Balachandran Manavalan & Gwang Lee. (2024) Unveiling local and global conformational changes and allosteric communications in SOD1 systems using molecular dynamics simulation and network analyses. Computers in Biology and Medicine 168, pages 107688.
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Blandine Madji Hounoum, Patrick Vourc’h, Romain Felix, Philippe Corcia, Franck Patin, Maxime Guéguinou, Marie Potier-Cartereau, Christophe Vandier, Cédric Raoul, Christian R. Andres, Sylvie Mavel & Hélène Blasco. (2016) NSC-34 Motor Neuron-Like Cells Are Unsuitable as Experimental Model for Glutamate-Mediated Excitotoxicity. Frontiers in Cellular Neuroscience 10.
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