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Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis.
No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: a tagging SNP approach.
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS.
A common haplotype within the PON1 promoter region is associated with sporadic ALS.
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery.
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS.
Polymorphism, Single Nucleotide
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden.
Polymorphism Single Nucleotide