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Identification of B6SJL mSOD1(G93A) mouse subgroups with different disease progression rates
Disease progression rates among patients with amyotrophic lateral sclerosis (ALS) vary greatly. While the majority of affected individuals survive three – five years following diagnosis, subgroups undergo a more rapidly progressing form, surviving less than one year, or slower progressing forms surv...
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| Izdano u: | J Comp Neurol |
|---|---|
| Glavni autori: | , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2015
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4607568/ https://ncbi.nlm.nih.gov/pubmed/26010802 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cne.23814 |
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