NOTCH3 variants in patients with suspected CADASIL

NOTCH3 variants in patients with suspected CADASIL

Background: Cerebral autosomal dominant arteriopathy with subcortical infarctions and leukoencephalopathy (CADASIL) is the most common hereditary form of cerebral small vessel disease. It is clinically, radiologically, and genetically heterogeneous and is caused by NOTCH3 mutations. Methods: In this...

Full description

Bibliographic Details
Main Authors: Orhan Gorukmez, Ozlem Gorukmez, Ali Topak, Meral Seferoglu, Ali O Sivaci, Asuman Ali, Nermin Tepe, Sibel C Kabay, Ozlem Taskapilioglu
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-01-01
Series:Annals of Indian Academy of Neurology
Subjects:
cadasil
ngs
notch3
Online Access:http://www.annalsofian.org/article.asp?issn=0972-2327;year=2023;volume=26;issue=4;spage=484;epage=490;aulast=Gorukmez

Internet

http://www.annalsofian.org/article.asp?issn=0972-2327;year=2023;volume=26;issue=4;spage=484;epage=490;aulast=Gorukmez

Similar Items