New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)-Reference-Cited by-同舟云学术

New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)

Published:2015-02 Issue:1-2 Volume:349 Page:196-201
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Abramycheva Natalya,Stepanova Maria,Kalashnikova Lyudmila,Zakharova Maria,Maximova Marina,Tanashyan Marine,Lagoda Olga,Fedotova Ekaterina,Klyushnikov Sergey,Konovalov Rodion,Sakharova Alla,Illarioshkin Sergey

Funder

Russian Foundation for Basic Research

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference42 articles.

1. CADASIL;Chabriat;Lancet Neurol,2009

2. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease;Choi;J Clin Neurol,2010

3. Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy;Tournier-Lasserve;Stroke,1991

4. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia;Joutel;Nature,1996

5. Hereditary cerebral small vessel diseases: a review;Federico;J Neurol Sci,2012

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