Naruse Yoshihisa | Department of Molecular Genetics
スポンサーリンク
概要
Department of Molecular Genetics | 論文
- PJ-015 Novel SCN5A Mutations Associated with Japanese Brugada Syndrome Patients(Arrhythmia, basic(04)(A),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- Increased DOI-Induced Wet-Dog Shakes in Adrenocorticotropic Hormone-Treated Rats Are Not Affected by Chronic Imipramine Treatment : Possible Involvement of Enhanced 5-HT_-Receptor Expression in the Frontal Cortex
- Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations?
- Paroxysmal movement disorders in severe myoclonic epilepsy in infancy