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Novel bi-allelic FBXO7 variants in a family with early-onset typical Parkinson's disease.
Keller Sarmiento, Ignacio J; Afshari, Mitra; Kinsley, Lisa; Silani, Vincenzo; Akhtar, Rizwan S; Simuni, Tanya; Lubbe, Steven J; Krainc, Dimitri; Mencacci, Niccolò E.
Afiliação
  • Keller Sarmiento IJ; Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
  • Afshari M; Division of Movement Disorders, Rush University Medical Center, and Biostatistical Analysis, Department of Neurological Sciences, Rush University Medical Center, Chicago, IL, USA.
  • Kinsley L; Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
  • Silani V; Department of Neurology and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan, Italy; Dino Ferrari Center, Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, 20122, Italy.
  • Akhtar RS; Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
  • Simuni T; Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
  • Lubbe SJ; Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
  • Krainc D; Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
  • Mencacci NE; Ken and Ruth Davee Department of Neurology and Simpson Querrey Center for Neurogenetics, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA. Electronic address: niccolo.mencacci@northwestern.edu.
Parkinsonism Relat Disord ; 104: 88-90, 2022 11.
Article em En | MEDLINE | ID: mdl-36274328
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Proteínas F-Box Limite: Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Proteínas F-Box Limite: Humans / Male Idioma: En Revista: Parkinsonism Relat Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos