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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Pubblicato in:J Comp Neurol
Autori principali: Haulcomb, Melissa M., Mesnard-Hoaglin, Nichole A., Batka, Richard J., Meadows, Rena M., Miller, Whitney M., McMillan, Kathryn P., Brown, Todd J., Sanders, Virginia M., Jones, Kathryn J.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2015
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Article
Accesso online: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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