Childhood, epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutationShow others and affiliations
2004 (English)In: Neurology, ISSN 0028-3878, E-ISSN 1526-632X, Vol. 63, no 6, p. 1136-1137Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. Vol. 63, no 6, p. 1136-1137
Keywords [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
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:uu:diva-66943PubMedID: 15452324OAI: oai:DiVA.org:uu-66943DiVA, id: diva2:94854
2005-09-262005-09-262017-11-28Bibliographically approved