MATSUO Muneaki | Department of Pediatrics, Faculty of Medicine, Saga University

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• Department of Pediatrics, Faculty of Medicine, Saga Universityの論文著者

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

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