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  • Carlsson, AnnaUmeå universitet,Umeå centrum för molekylär medicin (UCMM) (author)

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1

  • Article/chapterEnglish2002

Publisher, publication year, extent ...

  • Lippincott Williams & Wilkins,2002
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:liu-48709
  • https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-48709URI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-5099URI
  • https://doi.org/10.1212/01.WNL.0000036617.04943.96DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Migraine is the most common type of chronic episodic headache. To find novel susceptibility genes for familial migraine with and without aura, a genomewide screen was performed in a large family from northern Sweden. Evidence of linkage was obtained on chromosome 6p12.2-p21.1, with a maximum two-point lod score of 5.41 for marker D6S452. The patients with migraine shared a common haplotype of 10 Mb between markers D6S1650 and D6S1960.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Forsgren, LarsUmeå universitet,Klinisk neurovetenskap,Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden(Swepub:umu)lafo0001 (author)
  • Nylander, Per-OlofLinköpings universitet,Hälsouniversitetet,Psykiatri(Swepub:liu)perny42 (author)
  • Hellman, Urban,1966-Umeå universitet,Medicinsk och klinisk genetik,Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden(Swepub:umu)urhe0001 (author)
  • Forsman-Semb, KUmeå universitet,Medicinsk och klinisk genetik,Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden (author)
  • Holmgren, GUmeå universitet,Medicinsk och klinisk genetik,Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden (author)
  • Holmberg, DanUmeå universitet,Umeå centrum för molekylär medicin (UCMM),Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden(Swepub:umu)daho0001 (author)
  • Holmberg, MUmeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten) (author)
  • Umeå universitetUmeå centrum för molekylär medicin (UCMM) (creator_code:org_t)

Related titles

  • In:Neurology: Lippincott Williams & Wilkins59:11, s. 1804-18070028-38781526-632X

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