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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2004-8-26
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pubmed:abstractText |
Familial partial epilepsy with variable foci (FPEVF) is an autosomal dominant syndrome characterized by partial seizures originating from different brain regions in different family members in the absence of detectable structural abnormalities. A gene for FPEVF was mapped to chromosome 22q12 in two distantly related French-Canadian families.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0013-9580
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pubmed:author |
pubmed-author:AndermannEvaE,
pubmed-author:AndermannFrederickF,
pubmed-author:BerkovicSamuel FSF,
pubmed-author:Díaz-OteroFernandoF,
pubmed-author:DesbiensRichardR,
pubmed-author:DubeauFrancoisF,
pubmed-author:Fernández-BullidoYolandaY,
pubmed-author:Gómez-GarrePilarP,
pubmed-author:Lopes-CendesIsciaI,
pubmed-author:MartínMercedesM,
pubmed-author:MulleyJohn CJC,
pubmed-author:PandolfoMassimoM,
pubmed-author:PhillipsHilary AHA,
pubmed-author:SchefferIngrid EIE,
pubmed-author:SerratosaJose MJM,
pubmed-author:WallaceRobyn HRH,
pubmed-author:XiongLanL
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pubmed:copyrightInfo |
Copyright 2004 International League Against Epilepsy
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pubmed:issnType |
Print
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1054-60
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:15329069-Adolescent,
pubmed-meshheading:15329069-Adult,
pubmed-meshheading:15329069-Age of Onset,
pubmed-meshheading:15329069-Canada,
pubmed-meshheading:15329069-Child,
pubmed-meshheading:15329069-Chromosome Mapping,
pubmed-meshheading:15329069-Chromosomes, Human, Pair 22,
pubmed-meshheading:15329069-Diagnosis, Differential,
pubmed-meshheading:15329069-Epilepsies, Partial,
pubmed-meshheading:15329069-Epilepsy, Frontal Lobe,
pubmed-meshheading:15329069-Female,
pubmed-meshheading:15329069-Genetic Linkage,
pubmed-meshheading:15329069-Genetic Markers,
pubmed-meshheading:15329069-Haplotypes,
pubmed-meshheading:15329069-Humans,
pubmed-meshheading:15329069-Lod Score,
pubmed-meshheading:15329069-Male,
pubmed-meshheading:15329069-Pedigree,
pubmed-meshheading:15329069-Phenotype,
pubmed-meshheading:15329069-Spain
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pubmed:year |
2004
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pubmed:articleTitle |
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.
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pubmed:affiliation |
Epilepsy Research Centre, University of Melbourne, Austin & Repatriation Medical Centre, Victoria, Australia. s.berkovic@unimelb.edu.au
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pubmed:publicationType |
Journal Article,
Comparative Study
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