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Showing articles 0 to 2 of 2 Filter Applied: familial (Click to remove) Clinicopathologic Conference,Aceruloplasminemia, Hereditary NEJM 383:1974-1983, Case 35-2020, 2020 Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene NEJM 326:444-449, Medori,R.,et al, 1992 Showing articles 0 to 2 of 2