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Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

Mead, S; Uphill, J; Beck, J; Poulter, M; Campbell, T; Lowe, J; Adamson, G; (2012) Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. HUMAN MOLECULAR GENETICS , 21 (8) pp. 1897-1906. 10.1093/hmg/ddr607.

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Type: Article
Title: Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
DOI: 10.1093/hmg/ddr607
Keywords: Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Genetics & Heredity, BIOCHEMISTRY & MOLECULAR BIOLOGY, GENETICS & HEREDITY, CREUTZFELDT-JAKOB-DISEASE, PHENOTYPIC HETEROGENEITY, MOLECULAR ANALYSIS, INCUBATION-TIME, VARIANT CJD, MICE, SUSCEPTIBILITY, IDENTIFICATION, POLYMORPHISMS, UPSTREAM
UCL classification: UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Neurology
UCL > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Neurology > Neurodegenerative Diseases
UCL > School of Life and Medical Sciences > Faculty of Life Sciences
UCL > School of Life and Medical Sciences > Faculty of Life Sciences > Biosciences (Division of) > Genetics, Evolution and Environment > UCL Genetics Institute
URI: http://discovery.ucl.ac.uk/id/eprint/1335380
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