Archetypal <i>NOTCH3</i> 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

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.

Afiliación

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 en En | MEDLINE | ID: mdl-27844030

Texto completo

Añadir a Mi BVS

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Ann Clin Transl Neurol Año: 2016 Tipo del documento: Article