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Childhood, epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Neuroscience.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Neuroscience.
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2004 (English)In: Neurology, ISSN 0028-3878, E-ISSN 1526-632X, Vol. 63, no 6, 1136-1137 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. Vol. 63, no 6, 1136-1137 p.
Keyword [en]
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
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Medical and Health Sciences
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URN: urn:nbn:se:uu:diva-66943PubMedID: 15452324OAI: oai:DiVA.org:uu-66943DiVA: diva2:94854
Available from: 2005-09-26 Created: 2005-09-26 Last updated: 2017-11-28Bibliographically approved

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Melberg, AtleKumlien, EvaRaininko, RailiFlink, Roland

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