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Genet Med. 2018 Sep 20. doi: 10.1038/s41436-018-0306-z. [Epub ahead of print]

Correction: The effect of NOTCH3 pathogenic variant position on CADASIL disease severity: NOTCH3 EGFr 1-6 pathogenic variant are associated with a more severe phenotype and lower survival compared with EGFr 7-34 pathogenic variant.

Author information

1
CADASIL Research Group, Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands. j.w.rutten@lumc.nl.
2
Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands. j.w.rutten@lumc.nl.
3
CADASIL Research Group, Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
4
Institute for Stroke and Dementia Research, University Hospital (LMU), Munich, Germany.
5
Department of Neurology, AP-HP, Lariboisière Hospital, Paris, France.
6
Department of Neurology, SLK-Kliniken Heilbronn, Heilbronn, Germany.
7
"L. Sacco" Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
8
Department of Medicine, Surgery and Neurosciences, Medical School, University of Siena, Siena, Italy.
9
Stroke Research Group, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

Abstract

This Article was originally published under Nature Research's License to Publish, but has now been made available under a [CC BY 4.0] license. The PDF and HTML versions of the Article have been modified accordingly.

PMID:
30237574
DOI:
10.1038/s41436-018-0306-z
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