Amyotrophic lateral sclerosis type 20

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the HNRNPA1 gene.

Also known as: ALS20, HNRNPA1 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 20, amyotrophic lateral sclerosis caused by mutation in HNRNPA1, amyotrophic lateral sclerosis type 20

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