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Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation.
https://arctichealth.org/en/permalink/ahliterature30107
Source
Neurology. 2004 Sep 28;63(6):1136-7
Publication Type
Article
Date
Sep-28-2004
More detail
Author
E E Kors
A. Melberg
K R J Vanmolkot
E. Kumlien
J. Haan
R. Raininko
R. Flink
H B Ginjaar
R R Frants
M D Ferrari
A M J M van den Maagdenberg
Author Affiliation
Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Source
Neurology. 2004 Sep 28;63(6):1136-7
Date
Sep-28-2004
Language
English
Publication Type
Article
Keywords
Adult
Age of Onset
Amino Acid Substitution
Calcium Channels - genetics - physiology
Child
Child, Preschool
DNA Mutational Analysis
Disease Progression
Epilepsy, Complex Partial - genetics
Exons - genetics
Female
Haplotypes - genetics
Heterozygote
Humans
Male
Migraine with Aura - genetics
Migraine without Aura - genetics
Mutation, Missense
Pedigree
Point Mutation
Research Support, Non-U.S. Gov't
Spinocerebellar Degenerations - genetics
Sweden
PubMed ID
15452324
View in PubMed
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