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Article

Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.

Human genomics - 8 Jan 2016

Domitrz Izabela, Kosiorek Michalina, Żekanowski Cezary, Kamińska Anna

Abstract excerpt

BACKGROUND AND AIM: Migraine is the most common neurological disorder, affecting approximately 12 % of the adult population worldwide, caused by both environmental and genetic factors. Three causative genes have been identified in familial hemiplegic migraine (FHM) families: CACNA1A, ATP1A2, and SCNA1A. Recently, several mutations in KCNK18 have also been found as causative factors in migraine development. The...

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Identifiers

PMID: 26747084
DOI: 10.1186/s40246-015-0057-8
PMCID: PMC4706665

Genes

KCNK18

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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