Independent Occurrence of the CHRNA4 Ser248Phe Mutation in a Norwegian Family with Nocturnal Frontal Lobe Epilepsy
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概要
- 論文の詳細を見る
- 2000-05-01
著者
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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 Of Human Genetics University Hospital Bonn
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Steinlein Ortrud
Institute For Human Genetics Friedrich-wilhelms-university Of Bonn
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Steinlein Ortrud
Institut Fur Humangenetik Rheinische Friendrich-wilhelms-universitat
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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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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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Brodtkorb Eylert
Department Of Neurology Trondheim University Hospital
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Brodtkorb Eylert
Department Of Neurology And Clinical Neurophysiology St. Olav's Hospital
関連論文
- Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
- Chromosomal Abnormalities and Epilepsy : A Review for Clinicians and Gene Hunters
- Epilesies with single gene inheritance
- 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
- Autosomal Dominant Nocturnal Frontal Lobe Epilepsy : An Electroclinical Study of a Norwegian Family with Ten Affected Members
- Familial Temporal Lobe Epilepsy with Aphasic Seizures and Linkage to Chromosome 10q22-q24
- Speech-induced Aphasic Seizures in Epilepsy Caused by LGI1 Mutation
- Ethinyl Estradiol, Not Progestogens, Reduces Lamotrigine Serum Concentrations
- Asymmetry of Long-latency Auditory Evoked Potentials in LGI1-related Autosomal Dominant Lateral Temporal Lobe Epilepsy
- Levetiracetam Concentrations in Serum and in Breast Milk at Birth and during Lactation
- Idiopathic Epilepsies with a Monogenic Mode of Inheritance
- Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX