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...
Huvudupphovsmän: | Evans, M, Mr Matthew C Evans |
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Övriga upphovsmän: | Turner, M |
Materialtyp: | Lärdomsprov |
Språk: | English |
Publicerad: |
2012
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Ämnen: |
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