Modelling amyotrophic lateral sclerosis (ALS) using mutant and CAS9/CRISPR-corrected motor neurons from patients with C9ORF72 mutations reveals disease-specific cellular phenotypes

Autor: Mutihac, R., Ababneh, N., Scaber, J., Wade-Martins, R., Cowley, S., Talbot, K.
Zdroj: In Journal of the Neurological Sciences 15 October 2015 357 Supplement 1:e48-e48
Databáze: ScienceDirect
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