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4. The prion diseases. Brown K; Mastrianni JA J Geriatr Psychiatry Neurol; 2010 Dec; 23(4):277-98. PubMed ID: 20938044 [TBL] [Abstract][Full Text] [Related]
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10. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. Kitamoto T; Ohta M; Doh-ura K; Hitoshi S; Terao Y; Tateishi J Biochem Biophys Res Commun; 1993 Mar; 191(2):709-14. PubMed ID: 8461023 [TBL] [Abstract][Full Text] [Related]
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14. Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene. Mallucci GR; Campbell TA; Dickinson A; Beck J; Holt M; Plant G; de Pauw KW; Hakin RN; Clarke CE; Howell S; Davies-Jones GA; Lawden M; Smith CM; Ince P; Ironside JW; Bridges LR; Dean A; Weeks I; Collinge J Brain; 1999 Oct; 122 ( Pt 10)():1823-37. PubMed ID: 10506086 [TBL] [Abstract][Full Text] [Related]
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20. [Fatal familial insomnia: phenotypic changes determined by polymorphism of the codon 129]. Colombier C; Géraud G; Delisle MB; Laplanche JL; Pavy le Traon A; Alizé P; Delpla PA Rev Neurol (Paris); 1997 May; 153(4):239-43. PubMed ID: 9296141 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]