濱崎 雄平 | Department of Pediatrics, Faculty of Medicine, Saga University
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概要
Department of Pediatrics, Faculty of Medicine, Saga University | 論文
- Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese people
- In Vitro Cleavage of the MLL Gene by Topoisomerase II Inhibitor (Etoposide) in Normal Cord and Peripheral Blood Mononuclear Cells
- Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure
- Classic Rett syndrome in a boy with R133C mutation of MECP2
- Frequent association of autism spectrum disorder in patients with childhood onset epilepsy