Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Screen for CACNA1A and ATP1A2 mutations in sporadic hemiplegic migraine patients.

Cephalalgia : an international journal of headache - 1 Sept 2008

Thomsen L L, Oestergaard E, Bjornsson A, Stefansson H, Fasquel A C, Gulcher J, Stefansson K, Olesen J

Abstract excerpt

The aim of this study was to investigate the involvement of the CACNA1A and ATP1A2 gene in a population-based sample of sporadic hemiplegic migraine (SHM). Patients with SHM (n = 105) were identified in a nationwide search in the Danish population. We sequenced all exons and promoter regions of the CACNA1A and ATP1A2 genes in 100 patients with SHM to search for possible SHM mutations. Novel DNA variants were...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amino Acid Substitution
Share to Calcium Channels

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Consensus Sequence

Share to Hemiplegia

Share to Migraine Disorders

Share to Mutation, Missense

Share to Sequence Homology, Amino Acid

Share to Sodium-Potassium-Exchanging ATPase

Source

Identifiers

PMID: 18513263
DOI: 10.1111/j.1468-2982.2008.01599.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screen for CACNA1A and ATP1A2 mutations in sporadic hemiplegic migraine patients.PMID 18513263Read ↗

ATP1A2 mutations in 11 families with familial hemiplegic migraine.Semantic proximity Read ↗

Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants.Semantic proximity Read ↗

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraineSemantic proximity Read ↗

Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation.Semantic proximity Read ↗

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.Semantic proximity Read ↗

De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.Semantic proximity Read ↗

Screening of <scp><i>CACNA1A</i></scp> and <scp><i>ATP1A2</i></scp> genes in hemiplegic migraine: clinical, genetic, and functional studiesSemantic proximity Read ↗

Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches.Semantic proximity Read ↗

The genetic spectrum of a population-based sample of familial hemiplegic migraine.Semantic proximity Read ↗

CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report.Semantic proximity Read ↗

Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families.Semantic proximity Read ↗

Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I GenesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.