A recent genome-wide association study (GWAS) found significant association of six single nucleotide polymorphisms (SNPs) in the gene FLJ10986 with sporadic amyotrophic lateral sclerosis (SALS). Another independent GWAS reported significant association of one SNP in the gene inositol 1,4,5-triphosphate receptor 2 (ITPR2) with SALS. These studies provided conflicting results. We examined the six most significant SNPs in FLJ10986 and one SNP in ITPR2 in a large cohort consisting of 595 SALS cases and 681 controls ascertained from Germany. Our results did not provide evidence for the association of these SNPs with SALS, suggesting a possible population-specific effect for FLJ10986 and ITPR2 that do not modulate the risk for SALS in the German ...
Identification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided no...
dentification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided no...
Background: Approximately 90% of persons with amyotrophic lateral sclerosis (ALS) have the sporadic ...
Background Amyotrophic lateral sclerosis (ALS) is a devastating disease characterised by progressive...
Background Amyotrophic lateral sclerosis (ALS) is a devastating disease characterised by progressive...
BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a devastating disease characterised by progressiv...
A genome-wide association study (GWAS) using pooled DNA samples from 386 sporadic ALS patients and 5...
The single-nucleotide polymorphisms (SNPs) rs6700125 and rs6690993 in FGGY (FLJ10986) were recently ...
The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown, but genetic factors ar...
The cause of sporadic ALS is largely unknown, but genetic factors are thought to play a significant ...
Identification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided no...
Identification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided no...
dentification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided no...
Background: Approximately 90% of persons with amyotrophic lateral sclerosis (ALS) have the sporadic ...
Background Amyotrophic lateral sclerosis (ALS) is a devastating disease characterised by progressive...
Background Amyotrophic lateral sclerosis (ALS) is a devastating disease characterised by progressive...
BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a devastating disease characterised by progressiv...
A genome-wide association study (GWAS) using pooled DNA samples from 386 sporadic ALS patients and 5...
The single-nucleotide polymorphisms (SNPs) rs6700125 and rs6690993 in FGGY (FLJ10986) were recently ...
The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown, but genetic factors ar...
The cause of sporadic ALS is largely unknown, but genetic factors are thought to play a significant ...
Identification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided no...
Identification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided no...
dentification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided no...
Background: Approximately 90% of persons with amyotrophic lateral sclerosis (ALS) have the sporadic ...