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12. Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy. Dagvadorj A; Petersen RB; Lee HS; Cervenakova L; Shatunov A; Budka H; Brown P; Gambetti P; Goldfarb LG Ann Neurol; 2002 Sep; 52(3):355-9. PubMed ID: 12205650 [TBL] [Abstract][Full Text] [Related]
13. Prion protein conformation in a patient with sporadic fatal insomnia. Mastrianni JA; Nixon R; Layzer R; Telling GC; Han D; DeArmond SJ; Prusiner SB N Engl J Med; 1999 May; 340(21):1630-8. PubMed ID: 10341275 [No Abstract] [Full Text] [Related]
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15. The prion diseases. Mastrianni JA; Roos RP Semin Neurol; 2000; 20(3):337-52. PubMed ID: 11051298 [TBL] [Abstract][Full Text] [Related]
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17. Insomnia in prion diseases: sporadic and familial. Gambetti P; Parchi P N Engl J Med; 1999 May; 340(21):1675-7. PubMed ID: 10341282 [No Abstract] [Full Text] [Related]
18. 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]
19. A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family. Areškevičiūtė A; Høgh P; Bartoletti-Stella A; Melchior LC; Nielsen PR; Parchi P; Capellari S; Broholm H; Scheie D; Lund EL J Neuropathol Exp Neurol; 2019 Jul; 78(7):595-604. PubMed ID: 31107536 [TBL] [Abstract][Full Text] [Related]
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