Ratings
0
Nobody has rated this yet. Be the first!
Works
3
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
_portrait_(restored).jpg/500px-Santiago_Ramón_y_Cajal_(1852-1934)_portrait_(restored).jpg)