Copy number variants are frequent in genetic generalized epilepsy with intellectual disability

Mullen, Saul A., Carvill, Gemma L., Bellows, Susannah, Bayly, Marta A., Trucks, Holger, Lal, Dennis, Sander, Thoman, Berkovic, Samuel F., Dibbens, Leanne M., Scheffer, Ingrid E. and Mefford, Heather C. 2013, Copy number variants are frequent in genetic generalized epilepsy with intellectual disability, Neurology, vol. 81, no. 17, pp. 1507-1514, doi: 10.1212/WNL.0b013e3182a95829.


Title Copy number variants are frequent in genetic generalized epilepsy with intellectual disability
Author(s) Mullen, Saul A.
Carvill, Gemma L.
Bellows, Susannah
Bayly, Marta A.
Trucks, Holger
Lal, Dennis
Sander, Thoman
Berkovic, Samuel F.
Dibbens, Leanne M.
Scheffer, Ingrid E.
Mefford, Heather C.
Journal name Neurology
Volume number 81
Issue number 17
Start page 1507
End page 1514
Total pages 8
Publisher AAN Publications
Place of publication New York, N.Y.
Publication date 2013-10-22
ISSN 1526-632X
Keyword(s) Adolescent
Adult
Aged
Case-Control Studies
Child
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Cohort Studies
Comorbidity
DNA Copy Number Variations
Epilepsy, Generalized
Female
Genetic Testing
Humans
Intellectual Disability
Male
Middle Aged
Phenotype
Rubinstein-Taybi Syndrome
Seizures
Young Adult
Science & Technology
Life Sciences & Biomedicine
Clinical Neurology
Neurosciences & Neurology
15Q13.3 MICRODELETION SYNDROME
RECURRENT MICRODELETIONS
INCREASE RISK
HUMAN GENOME
SCHIZOPHRENIA
16P11.2
DISORDERS
DELETIONS
ENCEPHALOPATHIES
Language eng
DOI 10.1212/WNL.0b013e3182a95829
Field of Research 1103 Clinical Sciences
1109 Neurosciences
1702 Cognitive Science
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©2013, American Academy of Neurology
Persistent URL http://hdl.handle.net/10536/DRO/DU:30110665

Document type: Journal Article
Collections: Faculty of Health
School of Psychology
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