Mutation screening and association analysis of NOTCH3 p.R544C in patients with migraine with or without aura.

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Abstract

The role of the NOTCH3 p.R544C variant, the predominant variant of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in multiple East Asian regions, in migraine is unknown.

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Author and article information

Journal

Journal ID (iso-abbrev): Cephalalgia

Title: Cephalalgia : an international journal of headache

Publisher: SAGE Publications

ISSN (Electronic): 1468-2982

ISSN (Print): 0333-1024

Publication date (Electronic): Aug 2022

Volume: 42

Issue: 9

Affiliations

[1 ] Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan.

[2 ] College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.

[3 ] Brain Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan.

[4 ] Division of Translational Research, Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan.

[5 ] Department of Radiology, Taipei Veterans General Hospital, Taipei, Taiwan.

Article

DOI: 10.1177/03331024221080891

PubMed ID: 35302383

SO-VID: 025ae6c7-8bab-4886-9bcd-4ed60f4664e1

History

Keywords: single-nucleotide polymorphism,prevalence,migraine,CADASIL

Data availability:

Keywords: single-nucleotide polymorphism, prevalence, migraine, CADASIL

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