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63. Polymorphisms of the prion protein gene (PRNP) in a Serbian population. Dimitrijević R; Cadez I; Keckarević-Marković M; Keckarević D; Kecmanović M; Dobricić V; Savić-Pavićević D; Brajusković G; Romac S Int J Neurosci; 2010 Jul; 120(7):496-501. PubMed ID: 20583902 [TBL] [Abstract][Full Text] [Related]
64. Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity. Mead S; Poulter M; Beck J; Webb TE; Campbell TA; Linehan JM; Desbruslais M; Joiner S; Wadsworth JD; King A; Lantos P; Collinge J Brain; 2006 Sep; 129(Pt 9):2297-317. PubMed ID: 16923955 [TBL] [Abstract][Full Text] [Related]
65. Inherited prion disease with 4-octapeptide repeat insertion linked to valine at codon 129. Sánchez-Valle R; Yagüe J; Turón A; Aróstegui JI; Nos C; Rey MJ; Ferrer I; Gelpi E Brain; 2012 Apr; 135(Pt 4):e212. PubMed ID: 22300874 [No Abstract] [Full Text] [Related]
66. Mutations and polymorphisms in the prion protein gene. Palmer MS; Collinge J Hum Mutat; 1993; 2(3):168-73. PubMed ID: 8364585 [TBL] [Abstract][Full Text] [Related]
67. A case with a 120 base pair insertional mutation in the prion protein gene: the first case in Japan. Beck G; Kawano T; Naba I; Nishimura T; Sawada J; Hazama T J Neurol Neurosurg Psychiatry; 2005 May; 76(5):756-7. PubMed ID: 15834045 [No Abstract] [Full Text] [Related]
68. The influence of PRNP polymorphisms on human prion disease susceptibility: an update. Kobayashi A; Teruya K; Matsuura Y; Shirai T; Nakamura Y; Yamada M; Mizusawa H; Mohri S; Kitamoto T Acta Neuropathol; 2015 Aug; 130(2):159-70. PubMed ID: 26022925 [TBL] [Abstract][Full Text] [Related]
69. [Prion disease: a new class of neurodegenerative disorders]. van Gool WA; Hoogerwaard EM; Kuiper MA; Portegies P; Bolhuis PA Ned Tijdschr Geneeskd; 1995 Mar; 139(12):606-13. PubMed ID: 7700403 [No Abstract] [Full Text] [Related]
70. Genetics of human prion disease. Ridley RM; Baker HF Dev Biol Stand; 1993; 80():15-23. PubMed ID: 7903647 [TBL] [Abstract][Full Text] [Related]