Ratings
0
Nobody has rated this yet. Be the first!
Works
5
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
EEG functional network topology is associated with disability in patients with amyotrophic lateral sclerosis
Exome sequencing reveals VCP mutations as a cause of familial ALS
Progressive apraxia of speech in a patient with a C9orf72 mutation
