onr:"swepub:oai:DiVA.org:umu-15297"
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- Norberg, AnnaUmeå universitet,Medicinsk och klinisk genetik (author)
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.
- Article/chapterEnglish2006
Publisher, publication year, extent ...
- Elsevier BV,2006
- printrdacarrier
Numbers
- LIBRIS-ID:oai:DiVA.org:umu-15297
- https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-15297URI
- https://doi.org/10.1016/j.neulet.2005.11.039DOI
Supplementary language notes
- Language:English
Part of subdatabase
- SwePubSwePub
Classification
Subject headings and genre
- Blood Proteins/*genetics
- Calcium-Binding Proteins/*genetics
- Chromosome Aberrations
- Chromosomes; Human; Pair 6/*genetics
- DNA Mutational Analysis
- Female
- Gene Deletion
- Genetic Predisposition to Disease/epidemiology/*genetics
- Heterozygote
- Humans
- Incidence
- Male
- Membrane Glycoproteins/*genetics
- Metalloendopeptidases/*genetics
- Migraine Disorders/epidemiology/*genetics
- Multigene Family/genetics
- Pedigree
- Polymorphism; Single Nucleotide/genetics
- Sweden/epidemiology
Added entries (persons, corporate bodies, meetings, titles ...)
- Forsgren, LarsUmeå universitet,Neurologi(Swepub:umu)lafo0001 (author)
- Holmberg, DanUmeå universitet,Medicinsk och klinisk genetik(Swepub:umu)daho0001 (author)
- Holmberg, MonicaUmeå universitet,Medicinsk och klinisk genetik(Swepub:umu)moho0003 (author)
- Umeå universitetMedicinsk och klinisk genetik (creator_code:org_t)
Related titles
- In:Neuroscience Letters: Elsevier BV396:2, s. 137-1420304-39401872-7972
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