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Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome.
Muhle, Hiltrud; Mefford, Heather C; Obermeier, Tanja; von Spiczak, Sarah; Eichler, Evan E; Stephani, Ulrich; Sander, Thomas; Helbig, Ingo.
Affiliation
  • Muhle H; Department of Neuropediatrics, University Medical Center Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany. Muhle@pedneuro.uni-kiel.de
Epilepsia ; 52(12): e194-8, 2011 Dec.
Article in En | MEDLINE | ID: mdl-22050399
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 15 / Chromosome Aberrations / Chromosome Deletion / Epilepsy, Absence / Intellectual Disability Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: Epilepsia Year: 2011 Document type: Article Affiliation country: Germany Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 15 / Chromosome Aberrations / Chromosome Deletion / Epilepsy, Absence / Intellectual Disability Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: Epilepsia Year: 2011 Document type: Article Affiliation country: Germany Country of publication: United States