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Showing articles 0 to 2 of 2 Filter Applied: genetic linkage (Click to remove) 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 Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991 Showing articles 0 to 2 of 2