Amyotrophic lateral sclerosis type 15

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the UBQLN2 gene.

Also known as: ALS15, UBQLN2 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant, amyotrophic lateral sclerosis caused by mutation in UBQLN2, amyotrophic lateral sclerosis type 15, amyotrophic lateral sclerosis 15 with or without frontotemporal dementia

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