摘要 : Complex I deficiency, the most common cause of mitochondrial disorders, accounts for a variety of clinical symptoms and its genetic heterogeneity makes identification of the disease genes particularly tedious. Indeed, most of the ... 展开
作者 | Benit P Steffann J Lebon S Chretien D Kadhom N de Lonlay P Goldenberg A Dumez Y Dommergues M Rustin P Munnich A Rotig A |
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作者单位 | |
期刊名称 | 《Human Genetics》 |
总页数 | 4 |
语种/中图分类号 | 英语 / R3 |
关键词 | Leigh Disease Microsatellite Repeats Mitochondrial Diseases NADH NADPH Oxidoreductases Leigh病 微随体重复 NADH NADPH氧化还原酶类 |
馆藏号 | N2007EPST0000825 |