Inherited mtDNA variations are not strong risk factors in human prion disease.
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| Title: | Inherited mtDNA variations are not strong risk factors in human prion disease. |
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| Authors: | Hudson G; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, UK., Uphill J; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Hummerich H; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Blevins J; Department of Pathology, Case Western Reserve University, Cleveland, OH, USA., Gambetti P; Department of Pathology, Case Western Reserve University, Cleveland, OH, USA., Zerr I; Clinical Dementia Center, Department of Neurology, Georg-August University Göttingen, Göttingen, Germany; Center for Neuropathology and Prion Research, Ludwig-Maximilians-University Munich Munich, Germany., Collinge J; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK., Mead S; MRC Prion Unit, Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK. Electronic address: s.mead@prion.ucl.ac.uk., Chinnery PF; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, UK. |
| Source: | Neurobiology of aging [Neurobiol Aging] 2015 Oct; Vol. 36 (10), pp. 2908.e1-3. Date of Electronic Publication: 2015 Jul 10. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Elsevier Country of Publication: United States NLM ID: 8100437 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-1497 (Electronic) Linking ISSN: 01974580 NLM ISO Abbreviation: Neurobiol Aging Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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