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Volumn 65, Issue 8, 2007, Pages 1433-1437
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Familial prion disease (GSS, familial CJD, FFI)
a
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Author keywords
[No Author keywords available]
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Indexed keywords
CREUTZFELDT JAKOB DISEASE;
FATAL FAMILIAL INSOMNIA;
GENETICS;
GERSTMANN STRAUSSLER SCHEINKER SYNDROME;
HUMAN;
MUTATION;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PATHOPHYSIOLOGY;
PRION;
REVIEW;
SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY;
CREUTZFELDT-JAKOB SYNDROME;
GERSTMANN-STRAUSSLER-SCHEINKER DISEASE;
HUMANS;
INSOMNIA, FATAL FAMILIAL;
MAGNETIC RESONANCE IMAGING;
MUTATION;
PRIONS;
TOMOGRAPHY, EMISSION-COMPUTED, SINGLE-PHOTON;
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EID: 34548839927
PISSN: 00471852
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (5)
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References (11)
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