Searching for migraine genes: exclusion of 290 cM out of the whole human genome

Ital J Neurol Sci. 1997 Oct;18(5):277-82. doi: 10.1007/BF02083304.

Abstract

A linkage and association analysis was made on 14 Italian families with recurrent migraine. We analyzed five chromosomal regions surrounding the candidate genes 5HT1D (1p36.3-34.3), 5HT1B (6q13), 5HT2A (13q14-21), 5HT transporter (17q11.2-12), CACNLB1 (17q11.2-22) and FHM (19p13), using 29 DNA polymorphic markers. All two-point lod scores were negative, and the chi 2 sib-pair analyses were not significant, thus indicating the probable exclusion of these regions as sites of migraine genes in our population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Mapping
  • DNA / analysis
  • DNA / genetics
  • Genetic Linkage
  • Genome, Human*
  • Humans
  • Migraine Disorders / genetics*
  • Pedigree
  • Polymorphism, Genetic
  • Receptors, Serotonin / genetics

Substances

  • Receptors, Serotonin
  • DNA