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Article

No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree.

European journal of medical genetics - 1 Jan 2000

Curtain Robert, Tajouri Lotti, Lea Rod, MacMillan John, Griffiths Lyn

Abstract excerpt

The aim of this study was to investigate through direct sequencing the insulin receptor (INSR) gene in DNA samples from a migraine affected family previously showing linkage to chromosome 19p13 in an attempt to detect disease associated mutations. Migraine is a common debilitating disorder with a significant genetic component. At present, the number and type of genes involved in the common forms of migraine are...

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Share to Chromosomes, Human, Pair 19

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Migraine Disorders

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Share to Polymorphism, Single Nucleotide

Share to Receptor, Insulin

Source

Identifiers

PMID: 16473310
DOI: 10.1016/j.ejmg.2005.01.015

Genes

INSR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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