Kato Mitsuhiro | Department Of Mental Retardation And Birth Defect Research National Institute Of Neuroscience Nation
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Department Of Mental Retardation And Birth Defect Research National Institute Of Neuroscience Nation | 論文
- A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy
- Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene
- Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications
- IMPROVEMENT OF MYOCARDIAL Ischemia IN JEOPARDIZED AREA WITH A REMOTE AC BYPASS GRAFT EVALUATED BY STRESS MYOCARDIAL SCINTIGRAPHY : Radioisotope : PROCEEDINGS OF THE 50th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SOCIETY
- Flow Measurement around Flapping Dragonflies