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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat
Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD
No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease
Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels
Mild cognitive impairment--beyond controversies, towards a consensus: report of the International Working Group on Mild Cognitive Impairment
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
