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DCTN1 mutation associated parkinsonism: case series of three new families with perry syndrome.
Stoker, Thomas B; Dostal, Vaclav; Cochius, Jeffrey; Williams-Gray, Caroline H; Scherzer, Clemens R; Wang, Junhao; Liu, Ganqiang; Coyle-Gilchrist, Ian.
Afiliación
  • Stoker TB; Department of Neurology, Norfolk and Norwich University Hospital, Colney Lane, Norwich, UK. tbs26@cantab.net.
  • Dostal V; Department of Neurology, Norfolk and Norwich University Hospital, Colney Lane, Norwich, UK.
  • Cochius J; Department of Neurology, Norfolk and Norwich University Hospital, Colney Lane, Norwich, UK.
  • Williams-Gray CH; John Van Geest Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Scherzer CR; ADPA Center for Advanced Parkinson Research, Harvard Medical School, Brigham and Women's Hospital, Boston, MA, USA.
  • Wang J; Precision Neurology Program, Harvard Medical School, Brigham and Women's Hospital, Boston, MA, USA.
  • Liu G; Neurobiology Research Center, School of Medicine, Shenzhen Campus of Sun Yat-Sen University, Shenzhen, 518107, Guangdong, China.
  • Coyle-Gilchrist I; Neurobiology Research Center, School of Medicine, Shenzhen Campus of Sun Yat-Sen University, Shenzhen, 518107, Guangdong, China.
J Neurol ; 269(12): 6667-6672, 2022 12.
Article en En | MEDLINE | ID: mdl-35895135
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos Parkinsonianos / Hipoventilación Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: J Neurol Año: 2022 Tipo del documento: Article
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos Parkinsonianos / Hipoventilación Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: J Neurol Año: 2022 Tipo del documento: Article