Amyotrophic lateral sclerosis type 18

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the PFN1 gene.

Also known as: ALS18, PFN1 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 18, amyotrophic lateral sclerosis caused by mutation in PFN1, amyotrophic lateral sclerosis type 18

9 clinical trials for this condition and its sub-types.