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Accumulation of dysfunctional SOD1 protein in Parkinson's disease is not associated with mutations in the SOD1 gene.
Trist, Benjamin G; Fifita, Jennifer A; Freckleton, Sarah E; Hare, Dominic J; Lewis, Simon J G; Halliday, Glenda M; Blair, Ian P; Double, Kay L.
Afiliação
  • Trist BG; Discipline of Biomedical Science and Brain and Mind Centre, Sydney Medical School, The University of Sydney, Sydney, NSW, 2006, Australia.
  • Fifita JA; Faculty of Medicine and Health Sciences, Department of Biomedical Sciences, Macquarie University, Sydney, NSW, 2109, Australia.
  • Freckleton SE; Faculty of Medicine and Health Sciences, Department of Biomedical Sciences, Macquarie University, Sydney, NSW, 2109, Australia.
  • Hare DJ; The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, 3052, Australia.
  • Lewis SJG; Elemental Bio-Imaging Facility, University of Technology Sydney, Broadway, NSW, 2007, Australia.
  • Halliday GM; Department of Pathology, The University of Melbourne, Parkville, VIC, 3052, Australia.
  • Blair IP; Healthy Brain Ageing Program, University of Sydney, Sydney, NSW, 2006, Australia.
  • Double KL; Royal Prince Alfred Hospital, Camperdown, NSW, 2050, Australia.
Acta Neuropathol ; 135(1): 155-156, 2018 01.
Article em En | MEDLINE | ID: mdl-29052003
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Superóxido Dismutase-1 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Superóxido Dismutase-1 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article