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Childhood, epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation
- Kors, E. E. (author)
-
- Melberg, Atle (author)
- Uppsala universitet,Institutionen för neurovetenskap
- Vanmolkot, K. R. (author)
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- Haan, Jan (author)
- Ginjaar, H.B. (author)
- Frants, R.R. (author)
- Ferrari, M.D. (author)
- van den Maagdenberg, A. M. (author)
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- (creator_code:org_t)
- 2004
- 2004
- English.
- In: Neurology. - 0028-3878 .- 1526-632X. ; 63:6, s. 1136-1137
- Journal article (peer-reviewed)
Subject headings
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Keyword
- Adult
- Age of Onset
- Amino Acid Substitution
- Calcium Channels/genetics/*physiology
- Child
- Child; Preschool
- Classic Migraine/*genetics
- Common Migraine/genetics
- DNA Mutational Analysis
- Disease Progression
- Epilepsy; Complex Partial/*genetics
- Exons/genetics
- Female
- Haplotypes/genetics
- Heterozygote
- Humans
- Male
- Mutation; Missense
- Pedigree
- Point Mutation
- Research Support; Non-U.S. Gov't
- Spinocerebellar Degenerations/*genetics
- Sweden
- MEDICINE
- MEDICIN
Publication and Content Type
- ref (subject category)
- art (subject category)
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- Kors, E. E.
- Melberg, Atle
- Vanmolkot, K. R.
- Kumlien, Eva
- Haan, Jan
- Raininko, Raili
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- Flink, Roland
- Ginjaar, H.B.
- Frants, R.R.
- Ferrari, M.D.
- van den Maagdenb ...
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- Neurology
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- Uppsala University
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