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Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP).
Van den Broecke, Astrid; Decruyenaere, Alexander; Schuermans, Nika; Verdin, Hannah; Ghijsels, Jody; Sieben, Anne; Dermaut, Bart; Hemelsoet, Dimitri.
Afiliação
  • Van den Broecke A; Department of Neurology, Ghent University Hospital, Ghent, Belgium. astrid.vandenbroecke@uzgent.be.
  • Decruyenaere A; Department of Medical Oncology, Ghent University Hospital, Ghent, Belgium.
  • Schuermans N; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Verdin H; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
  • Ghijsels J; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Sieben A; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
  • Dermaut B; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Hemelsoet D; Department of Biomolecular Medicine, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.
J Neurol ; 271(1): 263-273, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37689591
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Príons / Síndrome de Creutzfeldt-Jakob / Doenças Priônicas Limite: Humans Idioma: En Revista: J Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Príons / Síndrome de Creutzfeldt-Jakob / Doenças Priônicas Limite: Humans Idioma: En Revista: J Neurol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica