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Article

Analysis of 3 common polymorphisms in the KCNK18 gene in an Australian Migraine case-control cohort.

Gene - 10 Oct 2013

Maher B H, Taylor M, Stuart S, Okolicsanyi R K, Roy B, Sutherland H G, Haupt L M, Griffiths L R

Abstract excerpt

Migraine is a common neurological disorder characterised by temporary disabling attacks of severe head pain and associated disturbances. There is significant evidence to suggest a genetic aetiology to the disease however few causal mutations have been conclusively linked to the migraine subtypes Migraine with (MA) or without Aura (MO). The Potassium Channel, Subfamily K, member 18 (KCNK18) gene, coding the...

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Source

Identifiers

PMID: 23911303
DOI: 10.1016/j.gene.2013.07.030

Genes

KCNK18

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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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