Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome.

Strehlow, Vincent; Swinkels, Marielle E M; Thomas, Rhys H; Rapps, Nora; Syrbe, Steffen; Dorn, Thomas; Lemke, Johannes R.

Afiliação

Strehlow V; Institute of Human Genetics, University Hospital and Clinics, Leipzig, Germany.
Swinkels ME; Department of Biomedical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.
Thomas RH; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK.
Rapps N; Department of Psychosomatic Medicine and Psychotherapy, Medical University Hospital Tübingen, Tübingen, Germany.
Syrbe S; Department of Women and Child Health, Hospital for Children and Adolescents, University Hospital and Clinics, Leipzig, Germany; Division of Child Neurology and Inherited Metabolic Diseases, Department of General Paediatrics, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelb
Dorn T; Swiss Epilepsy Center, Zurich, Switzerland.
Lemke JR; Institute of Human Genetics, University Hospital and Clinics, Leipzig, Germany.

Mol Syndromol ; 7(4): 239-246, 2016 Sep.

Article em En | MEDLINE | ID: mdl-27781034