Exploring neuroinflammatory processes in a mouse model of amyotrophic lateral sclerosis

<p>Amyotrophic lateral sclerosis (ALS) is a devastating degenerative disease, affecting both upper and lower motor neurons in the CNS. Around 10% of ALS cases are classed as familial, and around 20% of these are due to a mutation in the gene superoxide dismutase-1 (SOD1). The SOD1G93A mouse is...

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Bibliografische gegevens
Hoofdauteurs: Evans, M, Mr Matthew C Evans
Andere auteurs: Turner, M
Formaat: Thesis
Taal:English
Gepubliceerd in: 2012
Onderwerpen:

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