Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Microdeletion at chromosomal position 15q13.3 has been described in intellectual disability, autism spectrum disorders, schizophrenia and recently in idiopathic generalized epilepsy (IGE). Using independent IGE cohorts, we first aimed to confirm the association of 15q13.3 deletions and IGE. We then...

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Bibliografski detalji
Glavni autori: Dibbens, Leanne M., Mullen, Saul, Helbig, Ingo, Mefford, Heather C., Bayly, Marta A., Bellows, Susannah, Leu, Costin, Trucks, Holger, Obermeier, Tanja, Wittig, Michael, Franke, Andre, Caglayan, Hande, Yapici, Zuhal, Sander, Thomas, Eichler, Evan E., Scheffer, Ingrid E., Mulley, John C., Berkovic, Samuel F.
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2009
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Articles
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3465696/
https://ncbi.nlm.nih.gov/pubmed/19592580
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp311
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