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Benign familial infantile convulsions: Linkage to chromosome 16p12-q12 in 14 families

dc.contributor.authorHikel, C
dc.contributor.authorWeber, YG
dc.contributor.authorBerger, A
dc.contributor.authorMaier, S
dc.contributor.authorKarafyllakes, S
dc.contributor.authorMeyer, N
dc.contributor.authorFukuyama, Y
dc.contributor.authorHalbach, A
dc.contributor.authorKurlemann, G
dc.contributor.authorNeubauer, B
dc.contributor.authorOsawa, M
dc.contributor.authorPust, B
dc.contributor.authorRating, D
dc.contributor.authorSaito, K
dc.contributor.authorStephani, U
dc.contributor.authorTauer, U
dc.contributor.authorLehmann-Horn, F
dc.contributor.authorJurkat-Rott, K
dc.contributor.authorLerche, H
dc.contributor.authorBebek, Nerses
dc.date.accessioned2021-03-04T14:25:45Z
dc.date.available2021-03-04T14:25:45Z
dc.date.issued2004
dc.identifier.citationWeber Y., Berger A., Bebek N., Maier S., Karafyllakes S., Meyer N., Fukuyama Y., Halbach A., Hikel C., Kurlemann G., et al., "Benign familial infantile convulsions: Linkage to chromosome 16p12-q12 in 14 families", EPILEPSIA, cilt.45, sa.6, ss.601-609, 2004
dc.identifier.issn0013-9580
dc.identifier.otherav_818146a9-b7d0-4040-8be0-a6e9356ac20e
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/88264
dc.identifier.urihttps://doi.org/10.1111/j.0013-9580.2004.48203.x
dc.description.abstractPurpose: Benign familial infantile convulsions (BFIC) is a form of idiopathic epilepsy. It is characterized by clusters of afebrile seizures occurring around the sixth month of life. The disease has a benign course with a normal development and rare seizures in adulthood. Previous linkage analyses defined three susceptibility loci on chromosomes 19q12-q13.11, 16p12-q12, and 2q23-31. However, a responsible gene has not been identified. We studied linkage in 16 further BFIC families.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectNöroloji
dc.titleBenign familial infantile convulsions: Linkage to chromosome 16p12-q12 in 14 families
dc.typeMakale
dc.relation.journalEPILEPSIA
dc.contributor.department, ,
dc.identifier.volume45
dc.identifier.issue6
dc.identifier.startpage601
dc.identifier.endpage609
dc.contributor.firstauthorID60671


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