Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL-Reference-Cited by-同舟云学术

Archetypal NOTCH3 mutations frequent in public exome: implications for CADASIL

Published:2016-09-28 Issue:11 Volume:3 Page:844-853
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Rutten Julie W.¹²,Dauwerse Hans G.¹²,Gravesteijn Gido¹,Belzen Martine J.¹,Grond Jeroen³,Polke James M.⁴,Bernal‐Quiros Manuel⁴,Lesnik Oberstein Saskia A. J.¹

Affiliation:

1. Department of Clinical Genetics Leiden University Medical Center Leiden The Netherlands

2. Department of Human Genetics Leiden University Medical Center Leiden The Netherlands

3. Department of Radiology Leiden University Medical Center Leiden The Netherlands

4. Neurogenetics Unit National Hospital for Neurology and Neurosurgery London United Kingdom

Funder

ZonMw

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.344

Reference36 articles.

1. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

2. CADASIL

3. Changing clinical patterns and increasing prevalence in CADASIL

4. MRI correlates of cognitive decline in CADASIL

5. Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL

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