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2. Prion disease: A newly identified mutation in prion protein is associated with diarrhoea and autonomic neuropathy. Bible E Nat Rev Neurol; 2014 Jan; 10(1):2. PubMed ID: 24296653 [No Abstract] [Full Text] [Related]
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8. A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation. Tunnell E; Wollman R; Mallik S; Cortes CJ; Dearmond SJ; Mastrianni JA Neurology; 2008 Oct; 71(18):1431-8. PubMed ID: 18955686 [TBL] [Abstract][Full Text] [Related]
9. 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]
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11. Familial prion disease with a novel serine to isoleucine mutation at codon 132 of prion protein gene (PRNP). Hilton DA; Head MW; Singh VK; Bishop M; Ironside JW Neuropathol Appl Neurobiol; 2009 Feb; 35(1):111-5. PubMed ID: 19187063 [No Abstract] [Full Text] [Related]
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