Screening for NOTCH3 gene mutations among 151 consecutive Korean patients with acute ischemic stroke.

scientific article published on 30 November 2011

Screening for NOTCH3 gene mutations among 151 consecutive Korean patients with acute ischemic stroke. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.JSTROKECEREBROVASDIS.2011.10.013
P698PubMed publication ID22133740
P5875ResearchGate publication ID51846080

P2093author name stringJung Seok Lee
Jay Chol Choi
Keun-Hwa Lee
Ji-Hoon Kang
Sook-Keun Song
Sa-Yoon Kang
P433issue5
P304page(s)608-614
P577publication date2011-11-30
P1433published inJournal of Stroke and Cerebrovascular DiseasesQ15762579
P1476titleScreening for NOTCH3 gene mutations among 151 consecutive Korean patients with acute ischemic stroke.
P478volume22

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cites work (P2860)
Q53248522A Next-Generation Sequencing of the NOTCH3 and HTRA1 Genes in CADASIL Patients.
Q30861866CADASIL and CARASIL.
Q36288849Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects
Q51064066Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Phenotypic and mutational spectrum in patients from mainland China.
Q35754682Prevalence of CADASIL and Fabry Disease in a Cohort of MRI Defined Younger Onset Lacunar Stroke
Q37368347The Association Between the Genetic Variants of the NOTCH3 Gene and Ischemic Stroke Risk.
Q36922449The comparisons of phenotype and genotype between CADASIL and CADASIL-like patients and population-specific evaluation of CADASIL scale in China

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