The expansion of a hexanucleotide repeat GGGGCC in C9orf72 is the most common known cause of ALS accounting for ~ 40% familial cases and ~ 7% sporadic cases in the European population. In most people, the repeat length is 2, but in people with ALS, hundreds to thousands of repeats may be observed. A small proportion of people have an intermediate expansion, of the order of 20 to 30 repeats in size, and it remains unknown whether intermediate expansions confer risk of ALS in the same way that massive expansions do. We investigated the association of this intermediate repeat with ALS by performing a meta-analysis of four previously published studies and a new British/Alzheimer's Disease Neuroimaging Initiative dataset of 1295 cases and 613 co...
Background We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9...
Background: We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9...
It has been recently reported that a large proportion of patients with familial amyotrophic lateral ...
The expansion of a hexanucleotide repeat GGGGCC in C9orf72 is the most common known cause of ALS acc...
The expansion of a hexanucleotide repeat GGGGCC in C9orf72 is the most common known cause of ALS acc...
Abstract The hexanucleotide repeat expansion in intron 1 of the C9orf72 gene causes amyotrophic late...
We investigated a CAG trinucleotide repeat expansion in the ATXN2 gene in amyotrophic lateral sclero...
We investigated a CAG trinucleotide repeat expansion in the ATXN2 gene in amyotrophic lateral sclero...
AbstractAn intronic expansion of a hexanucleotide GGGGCC repeat in the C9ORF72 gene has recently bee...
AbstractAn expanded hexanucleotide repeat in the C9orf72 gene is the most common genetic cause of am...
C9orf72 is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal d...
Hexanucleotide repeat expansions in C9orf72 are a major cause of frontotemporal lobar degeneration (...
Item does not contain fulltextOBJECTIVE: To assess the frequency and phenotype of hexanucleotide rep...
We determined the frequency of C9orf72 repeat expansions in a large cohort of Belgian patients with ...
It has been recently reported that a large proportion of patients with familial amyotrophic lateral ...
Background We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9...
Background: We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9...
It has been recently reported that a large proportion of patients with familial amyotrophic lateral ...
The expansion of a hexanucleotide repeat GGGGCC in C9orf72 is the most common known cause of ALS acc...
The expansion of a hexanucleotide repeat GGGGCC in C9orf72 is the most common known cause of ALS acc...
Abstract The hexanucleotide repeat expansion in intron 1 of the C9orf72 gene causes amyotrophic late...
We investigated a CAG trinucleotide repeat expansion in the ATXN2 gene in amyotrophic lateral sclero...
We investigated a CAG trinucleotide repeat expansion in the ATXN2 gene in amyotrophic lateral sclero...
AbstractAn intronic expansion of a hexanucleotide GGGGCC repeat in the C9ORF72 gene has recently bee...
AbstractAn expanded hexanucleotide repeat in the C9orf72 gene is the most common genetic cause of am...
C9orf72 is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal d...
Hexanucleotide repeat expansions in C9orf72 are a major cause of frontotemporal lobar degeneration (...
Item does not contain fulltextOBJECTIVE: To assess the frequency and phenotype of hexanucleotide rep...
We determined the frequency of C9orf72 repeat expansions in a large cohort of Belgian patients with ...
It has been recently reported that a large proportion of patients with familial amyotrophic lateral ...
Background We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9...
Background: We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9...
It has been recently reported that a large proportion of patients with familial amyotrophic lateral ...