Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.

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Title: Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.
Authors: Balendra R; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Uphill J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Collinson C; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Druyeh R; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Adamson G; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Hummerich H; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Zerr I; Clinical Dementia Center, Department of Neurology, Georg-August University Göttingen, Göttingen, Germany.; German Center for Neurodegenerative Diseases, Gottingen, Germany., Gambetti P; Department of Pathology, Case Western Reserve University, Cleveland, OH, 44060, USA., Collinge J; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK., Mead S; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK. s.mead@prion.ucl.ac.uk.
Source: BMC medical genetics [BMC Med Genet] 2016 Apr 07; Vol. 17, pp. 28. Date of Electronic Publication: 2016 Apr 07.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350 (Electronic) Linking ISSN: 14712350 NLM ISO Abbreviation: BMC Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.
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  Data: <searchLink fieldCode="AU" term="%22Balendra+R%22">Balendra R</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>; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Collinson+C%22">Collinson C</searchLink>; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Druyeh+R%22">Druyeh R</searchLink>; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Adamson+G%22">Adamson G</searchLink>; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Hummerich+H%22">Hummerich H</searchLink>; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.<br /><searchLink fieldCode="AU" term="%22Zerr+I%22">Zerr I</searchLink>; Clinical Dementia Center, Department of Neurology, Georg-August University Göttingen, Göttingen, Germany.; German Center for Neurodegenerative Diseases, Gottingen, Germany.<br /><searchLink fieldCode="AU" term="%22Gambetti+P%22">Gambetti P</searchLink>; Department of Pathology, Case Western Reserve University, Cleveland, OH, 44060, USA.<br /><searchLink fieldCode="AU" term="%22Collinge+J%22">Collinge J</searchLink>; MRC Prion Unit and Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.<br /><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. s.mead@prion.ucl.ac.uk.
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  Data: <searchLink fieldCode="JN" term="%22100968552%22">BMC medical genetics</searchLink> [BMC Med Genet] 2016 Apr 07; Vol. 17, pp. 28. <i>Date of Electronic Publication: </i>2016 Apr 07.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>100968552 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1471-2350 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214712350%22">14712350 </searchLink><i>NLM ISO Abbreviation: </i>BMC Med Genet <i>Subsets: </i>MEDLINE
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              Text: 2016 Apr 07
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