DOI:
10.1055/s-00000019
Fortschritte der Neurologie · Psychiatrie
LinksClose Window
References
Medori R, Trischtler HJ, LeBlanc A. et al.
Fatal familial insomnia, a prion disease with a mutation at codon 178 of prion protein gene.
N Engl J Med 1992; 326: 444-449
Search in:
We do not assume any responsibility for the contents of the web pages of other providers.