Description
C9orf72 is present in ~ 40% of familial ALS and 8-10 % of sporadic ALS. It is the most common mutation related to ALS - far more common than SOD1 or TDP-43.
Creative Biolabs's Human iPSC-Derived Motor Neuron Progenitors from a female donor diagnosed with amyotrophic lateral sclerosis (ALS), also known as motor neuron disease (MND), carrying C9orf72 hexanucleotide expansion.