Molecular basis of severe myoclonic epilepsy in infancy

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概要

• 論文の詳細を見る
• 2009-05-01

著者

• Yamakawa Kazuhiro

  Laboratory of Neurogenetics, RIKEN, Brain Science Institute

• Yamakawa Kazuhiro

  Laboratory For Neurogenetics Riken Brain Science Institute

• Yamakawa Kazuhiro

  Laboratory For Neurogenetics Brain Science Institute Institute Of Physical And Chemical Research (ri

• YAMAKAWA Kazuhiro

  Laboratory for Neurogenetics, RIKEN Brain Science Institute

関連論文

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• Genetics of epilepsy : current status and perspectives
• Genetic abnormalities underlying familial epilepsy syndromes
• A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures
• Endocytosis in the Epithelial Cells of the Endolymphatic Sac
• Stimulus-Induced Behavior in F1 Hybrids of Seizure-Sensitive and Seizure-Resistant Gerbils(Neurobiology)
• Molecular basis of severe myoclonic epilepsy in infancy
• R133C and R168X mutations in Japanese Rett syndrome patients : a caution for misdiagnosis
• Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome

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