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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD
Extracellular Vesicles Isolated from Human Induced Pluripotent Stem Cell-Derived Neurons Contain a Transcriptional Network
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)
