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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
Smolders, Stefanie; Philtjens, Stéphanie; Crosiers, David; Sieben, Anne; Hens, Elisabeth; Heeman, Bavo; Van Mossevelde, Sara; Pals, Philippe; Asselbergh, Bob; Dos Santos Dias, Roberto; Vermeiren, Yannick; Vandenberghe, Rik; Engelborghs, Sebastiaan; De Deyn, Peter Paul; Martin, Jean-Jacques; Cras, Patrick; Annaert, Wim; Van Broeckhoven, Christine.
Affiliation
  • Smolders S; Center for Molecular Neurology, VIB, Antwerp, Belgium.
  • Philtjens S; Institute Born-Bunge, Antwerp, Belgium.
  • Crosiers D; University of Antwerp, Antwerp, Belgium.
  • Sieben A; Center for Molecular Neurology, VIB, Antwerp, Belgium.
  • Hens E; Institute Born-Bunge, Antwerp, Belgium.
  • Heeman B; University of Antwerp, Antwerp, Belgium.
  • Van Mossevelde S; Center for Molecular Neurology, VIB, Antwerp, Belgium.
  • Pals P; Institute Born-Bunge, Antwerp, Belgium.
  • Asselbergh B; University of Antwerp, Antwerp, Belgium.
  • Dos Santos Dias R; Department of Neurology, University Hospital Antwerp, Edegem, Belgium.
  • Vermeiren Y; Center for Molecular Neurology, VIB, Antwerp, Belgium.
  • Vandenberghe R; Institute Born-Bunge, Antwerp, Belgium.
  • Engelborghs S; Department of Neurology, University Hospital Ghent and University of Ghent, Ghent, Belgium.
  • De Deyn PP; Center for Molecular Neurology, VIB, Antwerp, Belgium.
  • Martin JJ; Institute Born-Bunge, Antwerp, Belgium.
  • Cras P; University of Antwerp, Antwerp, Belgium.
  • Annaert W; Department of Neurology, University Hospital Antwerp, Edegem, Belgium.
  • Van Broeckhoven C; Department of Neurology, Hospital Network Antwerp, Antwerp, Belgium.
Acta Neuropathol Commun ; 9(1): 25, 2021 02 12.
Article in En | MEDLINE | ID: mdl-33579389
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Proteins / Mutation, Missense / Lewy Body Disease / Heterozygote / Homozygote Type of study: Prognostic_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Acta Neuropathol Commun Year: 2021 Type: Article Affiliation country: Belgium
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Proteins / Mutation, Missense / Lewy Body Disease / Heterozygote / Homozygote Type of study: Prognostic_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Acta Neuropathol Commun Year: 2021 Type: Article Affiliation country: Belgium