Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree-Reference-Cited by-同舟云学术

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Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree

Published:2021-12-23 Issue:51 Volume:100 Page:e28141
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Luan Huiyan,Zhang Lei,Zhang Sijin,Zhang Meng

Funder

Department of Science and Technology of Jilin Province

Norman Bethune Program of Jilin University

Jilin Provincial Special Program for Health Research Talents

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference9 articles.

1. A sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management;Russell;Lancet Neurol,2011

2. Advances in genetics of migraine;Sutherland;J Headache Pain,2019

3. From genotype to phenotype: expanding the clinical spectrum of CACNA1A variants in the era of next generation sequencing;Indelicato;Front Neurol,2021

4. Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant;Angelini;Eur J Med Genet,2019

5. Localization and functional properties of a rat brain alpha 1A calcium channel reflect similarities to neuronal Q- and P-type channels;Stea;Proc Natl Acad Sci USA,1994

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Two pediatric patients with hemiplegic migraine presenting as acute encephalopathy: case reports and a literature review;Frontiers in Pediatrics;2023-07-28

2. Case Report: A Novel CACNA1A Mutation Caused Flunarizine-Responsive Type 2 Episodic Ataxia and Hemiplegic Migraine With Abnormal MRI of Cerebral White Matter;Frontiers in Neurology;2022-05-23

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