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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 14, Iss. 7-8, 2013-12 ,pp. : 635-637

Informa Healthcare

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TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation

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Mutant SOD1 alters the motor neuronal transcriptome: implications for familial ALS

By Kirby Janine  

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Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP)

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Temporal gene expression patterns in G93A/SOD1 mouse

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