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

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Title: Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Authors: Mead S; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK., Uphill J, Beck J, Poulter M, Campbell T, Lowe J, Adamson G, Hummerich H, Klopp N, Rückert IM, Wichmann HE, Azazi D, Plagnol V, Pako WH, Whitfield J, Alpers MP, Whittaker J, Balding DJ, Zerr I, Kretzschmar H, Collinge J
Source: Human molecular genetics [Hum Mol Genet] 2012 Apr 15; Vol. 21 (8), pp. 1897-906. Date of Electronic Publication: 2011 Dec 30.
Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
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  Data: <searchLink fieldCode="AU" term="%22Mead+S%22">Mead S</searchLink>; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Uphill+J%22">Uphill J</searchLink><br /><searchLink fieldCode="AU" term="%22Beck+J%22">Beck J</searchLink><br /><searchLink fieldCode="AU" term="%22Poulter+M%22">Poulter M</searchLink><br /><searchLink fieldCode="AU" term="%22Campbell+T%22">Campbell T</searchLink><br /><searchLink fieldCode="AU" term="%22Lowe+J%22">Lowe J</searchLink><br /><searchLink fieldCode="AU" term="%22Adamson+G%22">Adamson G</searchLink><br /><searchLink fieldCode="AU" term="%22Hummerich+H%22">Hummerich H</searchLink><br /><searchLink fieldCode="AU" term="%22Klopp+N%22">Klopp N</searchLink><br /><searchLink fieldCode="AU" term="%22Rückert+IM%22">Rückert IM</searchLink><br /><searchLink fieldCode="AU" term="%22Wichmann+HE%22">Wichmann HE</searchLink><br /><searchLink fieldCode="AU" term="%22Azazi+D%22">Azazi D</searchLink><br /><searchLink fieldCode="AU" term="%22Plagnol+V%22">Plagnol V</searchLink><br /><searchLink fieldCode="AU" term="%22Pako+WH%22">Pako WH</searchLink><br /><searchLink fieldCode="AU" term="%22Whitfield+J%22">Whitfield J</searchLink><br /><searchLink fieldCode="AU" term="%22Alpers+MP%22">Alpers MP</searchLink><br /><searchLink fieldCode="AU" term="%22Whittaker+J%22">Whittaker J</searchLink><br /><searchLink fieldCode="AU" term="%22Balding+DJ%22">Balding DJ</searchLink><br /><searchLink fieldCode="AU" term="%22Zerr+I%22">Zerr I</searchLink><br /><searchLink fieldCode="AU" term="%22Kretzschmar+H%22">Kretzschmar H</searchLink><br /><searchLink fieldCode="AU" term="%22Collinge+J%22">Collinge J</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2012 Apr 15; Vol. 21 (8), pp. 1897-906. <i>Date of Electronic Publication: </i>2011 Dec 30.
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  Data: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=22210626
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        Value: 10.1093/hmg/ddr607
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              Text: 2012 Apr 15
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