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Relationship between C9orf72 repeat size and clinical phenotype.
Van Mossevelde, Sara; van der Zee, Julie; Cruts, Marc; Van Broeckhoven, Christine.
Afiliação
  • Van Mossevelde S; Center for Molecular Neurology, VIB, Universiteitsplein 1, 2610 Antwerp, Belgium; Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium; Department of Neurology and Memory Clinic, Hospital Network Antwerp Hoge Beuken, Commandant Weynsst
  • van der Zee J; Center for Molecular Neurology, VIB, Universiteitsplein 1, 2610 Antwerp, Belgium; Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.
  • Cruts M; Center for Molecular Neurology, VIB, Universiteitsplein 1, 2610 Antwerp, Belgium; Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.
  • Van Broeckhoven C; Center for Molecular Neurology, VIB, Universiteitsplein 1, 2610 Antwerp, Belgium; Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium. Electronic address: christine.vanbroeckhoven@molgen.vib-ua.be.
Curr Opin Genet Dev ; 44: 117-124, 2017 Jun.
Article em En | MEDLINE | ID: mdl-28319737
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Expansão das Repetições de DNA / Demência Frontotemporal / Proteína C9orf72 / Esclerose Lateral Amiotrófica / Degeneração Neural Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Expansão das Repetições de DNA / Demência Frontotemporal / Proteína C9orf72 / Esclerose Lateral Amiotrófica / Degeneração Neural Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article