摘要 : Sequence analysis of mitochondrial and nuclear candidate genes of complex I in children with deficiency of this complex and exhibiting Leigh-like syndrome has revealed, in one of them, a novel mutation in the NDUFS4 gene encoding ... 展开
作者 | Petruzzella V Vergari R Puzziferri I Boffoli D Lamantea E Zeviani M Papa S |
---|---|
作者单位 | |
期刊名称 | 《Human Molecular Genetics》 |
总页数 | 7 |
语种/中图分类号 | 英语 / R394 |
关键词 | Codon Nonsense Leigh Disease NADH NADPH Oxidoreductases DNA Complementary 密码子 无义 Leigh病 NADH NADPH氧化还原酶类 |
馆藏号 | N2007EPST0000828 |