黒田 康久 | Department of Physiology
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概要
Department of Physiology | 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)
- Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome : pathological mutations and polymorphisms
- Analysis of Ictal EEGs of Epilepsy Associated with Tuberous Sclerosis
- Relationship between severity of epilepsy and developmental outcome in Angelman syndrome
- Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations?