Discover Community Create You

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

Novel mutation of SLC20A2 in an Italian patient presenting with migraine.

Journal of neurology - 1 Oct 2014

Rubino Elisa, Giorgio Elisa, Gallone Salvatore, Pinessi Lorenzo, Orsi Laura, Gentile Salvatore, Duca Sergio, Brusco Alfredo

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Brain
Share to DNA Mutational Analysis
Share to Italy
Share to Migraine Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Sodium-Phosphate Cotransporter Proteins, Type III

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 25178512
DOI: 10.1007/s00415-014-7475-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel mutation of SLC20A2 in an Italian patient presenting with migraine.PMID 25178512Read ↗

A novel SLC20A2 mutation presenting with paroxysmal kinesigenic dyskinesia and epilepsy in a Chinese patient: a case report.Semantic proximity Read ↗

Functional characterization of a novel C-terminal <i>ATP1A2</i> mutation causing hemiplegic migraine and epilepsySemantic proximity Read ↗

A wide clinical phenotype spectrum in patients with ATP1A2 mutations.Semantic proximity Read ↗

Functional characterization of a novel PRRT2 variant found in a Portuguese patient with hemiplegic migraine.Semantic proximity Read ↗

Novel Lys215Asn mutation in an Italian family with Thomsen myotonia.Semantic proximity Read ↗

A SLC20A2 mutation identified in an asymptomatic patient with brain calcification.Semantic proximity Read ↗

Expanding the phenotype associated with biallelic SLC20A2 variants.Semantic proximity Read ↗

Novel heterozygous mutation of SLC12A3 gene in Gitelman syndrome.Semantic proximity Read ↗

De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report.Semantic proximity Read ↗

A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome.Semantic proximity Read ↗

PharmGKB submission update: V. PMT submissions of genetic variation in SLC22 family transporters.Semantic proximity Read ↗

SLC20A2 mutation manifesting as very late-onset orofacial dyskinesia.Semantic proximity Read ↗

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