Home > Genetic prion disease caused by PRNP Q160X mutation presenting with an orbitofrontal syndrome, cyclic diarrhea, and peripheral neuropathy
Genetic prion disease caused by PRNP Q160X mutation presenting with an orbitofrontal syndrome, cyclic diarrhea, and peripheral neuropathy
Manuscript Number:
16-0300R1
Author(s):
Jee Bang, Giovanni Coppola, Jamie C. Fong, Sven Forner, Michael D. Geschwind, Carrie K. Grouse, Anna M. Karydas, Andrea Legati, Bruce L. Miller, Zachary A. Miller, Jeffrey Ralph, Katherine J. Rankin, Julio C. Rojas
