Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome

15q13.3 microdeletions are the most common genetic findings identified in idiopathic generalized epilepsies to date, and they are present in up to 1% of patients. In addition, 15q13.3 microdeletions have been described in patients with epilepsy as part of a complex neurodevelopmental phenotype. We a...

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Detalles Bibliográficos
Autores principales: Muhle, Hiltrud, Mefford, Heather C, Obermeier, Tanja, von Spiczak, Sarah, Eichler, Evan E, Stephani, Ulrich, Sander, Thomas, Helbig, Ingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3270691/
https://www.ncbi.nlm.nih.gov/pubmed/22050399
http://dx.doi.org/10.1111/j.1528-1167.2011.03301.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3270691/
https://www.ncbi.nlm.nih.gov/pubmed/22050399
http://dx.doi.org/10.1111/j.1528-1167.2011.03301.x

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