Author:
Feucht Martha,Fuchs Karoline,Pichlbauer Ernest,Hornik Kurt,Scharfetter Joachim,Goessler Ralph,Füreder Thomas,Cvetkovic Nevenka,Sieghart Werner,Kasper Siegfried,Aschauer Harald
Reference40 articles.
1. Severe epilepsy in a patient with Prader–Willi syndrome due to a inversion-duplication of chromosome 15q11–13. A clinical, neurophysiological and molecular genetic study (abstract);Aguglia;Epilepsia,1995
2. Genetic aspects of the epilepsies;Andermann,1985
3. Developmental changes in human GABAA receptor subunit composition;Brooks-Kayal;Ann Neurol,1993
4. Duplication of 15q11–13 region in a patient with autism, epilepsy and ataxia;Bundey;Dev Med Child Neurol,1994
5. Proposal for revised classification of epilepsies and epileptic syndromes;Epilepsia,1989
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