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Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL.
Rutten, Julie W; Dauwerse, Hans G; Gravesteijn, Gido; van Belzen, Martine J; van der Grond, Jeroen; Polke, James M; Bernal-Quiros, Manuel; Lesnik Oberstein, Saskia A J.
Affiliation
  • Rutten JW; Department of Clinical Genetics Leiden University Medical Center Leiden The Netherlands; Department of Human Genetics Leiden University Medical Center Leiden The Netherlands.
  • Dauwerse HG; Department of Clinical Genetics Leiden University Medical Center Leiden The Netherlands; Department of Human Genetics Leiden University Medical Center Leiden The Netherlands.
  • Gravesteijn G; Department of Clinical Genetics Leiden University Medical Center Leiden The Netherlands.
  • van Belzen MJ; Department of Clinical Genetics Leiden University Medical Center Leiden The Netherlands.
  • van der Grond J; Department of Radiology Leiden University Medical Center Leiden The Netherlands.
  • Polke JM; Neurogenetics Unit National Hospital for Neurology and Neurosurgery London United Kingdom.
  • Bernal-Quiros M; Neurogenetics Unit National Hospital for Neurology and Neurosurgery London United Kingdom.
  • Lesnik Oberstein SA; Department of Clinical Genetics Leiden University Medical Center Leiden The Netherlands.
Ann Clin Transl Neurol ; 3(11): 844-853, 2016 11.
Article de En | MEDLINE | ID: mdl-27844030
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Risk_factors_studies Langue: En Journal: Ann Clin Transl Neurol Année: 2016 Type de document: Article
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Risk_factors_studies Langue: En Journal: Ann Clin Transl Neurol Année: 2016 Type de document: Article