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

Epilepsia

Volumn 52, Issue 12, 2011, Pages

  Muhle, Hiltrud ^a   Mefford, Heather C ^b   Obermeier, Tanja ^a   Von Spiczak, Sarah ^a   Eichler, Evan E ^c   Stephani, Ulrich ^a   Sander, Thomas ^d   Helbig, Ingo ^a  

^a UNIVERSITY OF KIEL   (Germany)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^c HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^d UNIVERSITY OF COLOGNE   (Germany)

Author keywords

Idiopathic generalized epilepsy; Intellectual disability

Indexed keywords

CLONAZEPAM; ETHOSUXIMIDE; VALPROIC ACID;

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 15Q; CHROMOSOME DELETION; COMPARATIVE GENOMIC HYBRIDIZATION; ELECTROENCEPHALOGRAM; EPILEPSY; FEMALE; GENETIC SCREENING; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MALE; PEDIATRIC EPILEPSY; PEDIGREE ANALYSIS; PHENOTYPE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; COHORT STUDIES; ELECTROENCEPHALOGRAPHY; EPILEPSY, ABSENCE; FEMALE; GENETIC TESTING; HUMANS; INTELLECTUAL DISABILITY; MAGNETIC RESONANCE IMAGING; MALE; NUCLEIC ACID HYBRIDIZATION; PEDIGREE; YOUNG ADULT;

EID: 82955232421     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2011.03301.x     Document Type: Article

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