Comment on

• Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.

  Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P, et al. Medori R, et al. N Engl J Med. 1992 Feb 13;326(7):444-9. doi: 10.1056/NEJM199202133260704. N Engl J Med. 1992. PMID: 1346338 Free PMC article.