Frontotemporal dementia and/or amyotrophic lateral sclerosis 7

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the CHMP2B gene.

Also known as: CHMP2B amyotrophic lateral sclerosis, CHMP2B-related amyotrophic lateral sclerosis, FTD3, amyotrophic lateral sclerosis caused by mutation in CHMP2B, amyotrophic lateral sclerosis, Chmp2B-related, frontotemporal dementia, chromosome 3-linked, Dmt1, dementia, familial nonspecific

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