C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia.

Objective: To further assess the presence of a large hexanucleotide repeat expansion in the first intron of the C9orf72 gene identified as the genetic cause of chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia (c9ALS/FTD) in 4 unrelated families with a conclusive linkage to c9ALS/FTD.

Methods: A repeat-primed polymerase chain reaction assay. Methods: Academic research. Methods: Affected and unaffected individuals from 4 ALS/FTD families. Methods: The amplified C9orf72 repeat expansion.

Results: We show that the repeat is expanded in and segregated perfectly with the disease in these 4 pedigrees.

Conclusions: Our findings further confirm the C9orf72 hexanucleotide repeat expansion as the causative mutation for c9ALS/FTD and strengthen the hypothesis that ALS and FTD belong to the same disease spectrum.