Steinlein Ortrud | Institute Of Human Genetics University Hospital Bonn
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概要
関連著者
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Steinlein Ortrud
Institute Of Human Genetics University Hospital Bonn
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Steinlein Ortrud
Institut Fur Humangenetik Rheinische Friendrich-wilhelms-universitat
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Berkovic Sam
Department Of Neurology University Of Melbourne Austin And Repatriation Medical Centre And Royal Chi
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Steinlein Ortrud
Institute For Human Genetics Friedrich-wilhelms-university Of Bonn
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Scheffer Ingrid
Department Of Medicine The University Of Melbourne Austin Health
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Scheffer Ingrid
Department Of Medicine (neurology) Royal Children's Hospital And Monash Medical Centre Austin A
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Scheffer Ingrid
Department Of Neurology University Of Melbourne Austin And Repatriation Medical Centre And Royal Chi
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Bertrand Daniel
Department Of Physiology Cmu
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Hufnagel Andreas
Department Of Epileptology University Of Bonn
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STOODT Jens
Institute for Human Genetics, Friedrich-Wilhelms-University of Bonn
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MULEEY John
Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital and Department of
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BRODTKORB Eylert
Department of Neurology, Trondheim University Hospital
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Stoodt Jens
Institute For Human Genetics Friedrich-wilhelms-university Of Bonn
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Muleey John
Department Of Cytogenetics And Molecular Genetics Women's And Children's Hospital And Depa
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LENIGER Tobias
Department of Neurology, University of Essen
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KANANURA Colette
Institute of Human Genetics, University Hospital Bonn
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BERTRAND Sonia
Department of Physiology, CMU
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Brodtkorb Eylert
Department Of Neurology Trondheim University Hospital
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Brodtkorb Eylert
Department Of Neurology And Clinical Neurophysiology St. Olav's Hospital
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Bertrand Sonia
Department Of Physiology Cmu
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Leniger Tobias
Department Of Neurology University Of Essen Essen
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Leniger Tobias
Department Of Neurology Department Of Psychiatry And Psychotherapy University Of Essen
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Kananura Colette
Institute Of Human Genetics University Hospital Bonn
著作論文
- Independent Occurrence of the CHRNA4 Ser248Phe Mutation in a Norwegian Family with Nocturnal Frontal Lobe Epilepsy
- A New Chrna4 Mutation with Low Penetrance in Nocturnal Frontal Lobe Epilepsy