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Article

Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG.

Neuroscience letters - 27 Mar 2006

Norberg Anna, Forsgren Lars, Holmberg Dan, Holmberg Monica

Abstract excerpt

Migraine is a complex, multifactorial disorder for which several loci have been identified in the human genome. We have previously reported linkage to a 10 Mb-region on chromosome 6p12.2-p21.1 in one large Swedish pedigree involving migraine with and without aura. To further investigate this cand...

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Source

Identifiers

PMID: 16378686
DOI: 10.1016/j.neulet.2005.11.039

Genes

EFHC1
RHAG
TNFRSF21

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16378686-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG.PMID 16378686Read ↗

Mutation analyses of genes on 6p12-p11 in patients with juvenile myoclonic epilepsy.Semantic proximity Read ↗

Heterogeneity at the JME 6p11-12 locus: absence of mutations in the EFHC1 gene in linked Dutch families.Semantic proximity Read ↗

DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.Semantic proximity Read ↗

A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.Semantic proximity Read ↗

EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality.Semantic proximity Read ↗

Mutational Analysis of Myoclonin1 Gene in Pakistani Juvenile Myoclonic Epilepsy Patients.Semantic proximity Read ↗

EFHC1 gene mutation profile of Turkish JME patients and its association with disease risk.Semantic proximity Read ↗

Intractable epilepsy of infancy due to homozygous mutation in the EFHC1 gene.Semantic proximity Read ↗

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.Semantic proximity Read ↗

Juvenile myoclonic epilepsy as a possible neurodevelopmental disease: role of EFHC1 or Myoclonin1.Semantic proximity Read ↗

Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry.Semantic proximity Read ↗

Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.Semantic proximity Read ↗

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