DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Medori R, Tritschler HJ, LeBlanc A. , et al.
Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.
N Engl J Med 1992;
326 (07) 444-449
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