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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
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
Novel PS1 mutation in a Bavarian kindred with familial Alzheimer disease.
Genetic complexity of Alzheimer's disease: successes and challenges.
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
