Idiopathic Epilepsies with a Monogenic Mode of Inheritance
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概要
- 論文の詳細を見る
- 1999-03-01
著者
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Steinlein Ortrud
Institute Of Human Genetics
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Steinlein Ortrud
Institut Fur Humangenetik Rheinische Friendrich-wilhelms-universitat
関連論文
- 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
- 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
- Asymmetry of Long-latency Auditory Evoked Potentials in LGI1-related Autosomal Dominant Lateral Temporal Lobe Epilepsy
- Idiopathic Epilepsies with a Monogenic Mode of Inheritance