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线粒体DNA突变与肾小管间质疾病 被引量:1

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摘要 粒体DNA是细胞中唯一的核外遗传物质,当其发生突变时,可使线粒体氧化磷酸化产能障碍,ATP合成减少。肾小管上皮细胞的物质转运需要足够的能量供应,因此。
作者 赵青 刘必成
出处 《国外医学(泌尿系统分册)》 2000年第1期23-25,共3页 Foreign Medical Sciences(Urology and Nephrology Foreign Medical Sciences)
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参考文献5

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同被引文献21

  • 1张丽珊,陈建明.线粒体DNA突变与人类疾病[J].国外医学(遗传学分册),1995,18(1):3-7. 被引量:10
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  • 6Kurogouchi F,Oguchi T,Mawatari E,et al.A case of mitochondrial cytopathy with a typical point mutation for MELAS,presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation.Am J Nephrol,1998,18(6 ):551-556
  • 7Doleris LM,Hill GS,Chedin P,et al.Focal segmental glomerulosclerosis associated with mitochondrial cytopathy.Kidney Int,2000,58:1851-1858
  • 8Hotta O,Inoue CN,Miyabayashi S,et al.Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNA Leu(UUR) gene mutation.Kidney Int,2001,59:1236-1243
  • 9Lee YS,Yap HK,Barshop BA,et al.Mitochondrial tubulopathy :the many faces of mitochondrial disorders.Pediatr Nephrol,2001,16(9):710-712
  • 10Wang LC,Lee WT,Tsai WY,et al.Mitochondrial cytopathy combined with Fanconi's syndrome.Pediatr Neurol,2000,22:403-406

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