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线粒体基因突变糖尿病的临床识别及诊断 被引量:1

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作者 于萌
出处 《辽宁实用糖尿病杂志》 2004年第1期11-13,共3页 Liaoning Journal of Practical Diabetology
  • 相关文献

参考文献6

  • 1[1]Anderson S,Bankier AT,Barrell BG,et al.Seguence and organization of the human mitochondrial genome.Nature 1981;290:457.
  • 2于萌,端木志强,齐今吾.线粒体基因突变与糖尿病[J].中国冶金工业医学杂志,1999,16(2):121-123. 被引量:2
  • 3[3]Van den Ouweland JMW,Lemkers HHPJ.Ruitenbeek W,et al.Mutation in mitoehondrial tRNAlett(UUR)gene in a large pedigrea with mater- nally transmitted type Ⅱ diabetes mellitus and deafness.Nature Gennetics 1992;1:368-371.
  • 4[4]Ballinger SW,Shoffner J M,Headays EV.et al.Maternally rahs mitted diabetes and deafness associated with 10.4kb mitochondtial DNA deletion.Nature with Nature Genetics 1992;1:11-15.
  • 5项坤三,王延庆,吴松华,陆惠娟,郑泰山,孙多奇,翁青,贾伟平,沈卫平,浦鎏,何进卫.线粒体tRNA^(Leu(UUR))基因突变糖尿病──患病率估测、临床特点及基因诊断途径[J].中国糖尿病杂志,1995,3(3):129-135. 被引量:34
  • 6[7]Van den Ouweland JMW,Lemkes HHPJ,Richatd C,et al.Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associated with a single point mutation m the mitochondrial tRNAlett(UUR)gene.Diabetes 1994;43:746-751.

二级参考文献1

  • 1项坤三 王延庆 等.线粒体tRNA^leu(uuR)基因突变糖尿病--患病率估测,临床特点及基因诊断途径[J].中国糖尿病杂志,1995,3:129-129.

共引文献33

同被引文献19

  • 1项坤三,陆惠娟,吴松华,郑泰山,孙多奇,王延庆,贾伟平,钱荣立,翁青,沈卫平,何进卫,严钱勤,浦鎏,何海屏.线粒体tRNA^(Leu(UUR))基因突变糖尿病的基因诊断[J].中华医学杂志,1995,75(4):216-219. 被引量:44
  • 2项坤三,王延庆,吴松华,陆惠娟,郑泰山,孙多奇,翁青,贾伟平,沈卫平,浦鎏,何进卫.线粒体tRNA^(Leu(UUR))基因突变糖尿病──患病率估测、临床特点及基因诊断途径[J].中国糖尿病杂志,1995,3(3):129-135. 被引量:34
  • 3[1]ANDERSON S,BANKIERr A T,BARREL B G,et al.Seguence and organization of the human mitochondrial genome[J].Nature,1981,290:457-460.
  • 4[2]LINNANE A W.,MARZUKE S,OZAWA T,et al.Mitochondrial DAN mutation as contributor to agaig and degenerative diseases[J].Lancet,1989,1:642-645.
  • 5[3]TRISLER H,MEDORIR.Mitochondrial DNA alteration as a source of human disorders[J].Neurology,1993,43:280-284.
  • 6[4]GERBITA K O.Does the mitochondrial DNA play a role in the pathogenesis of diseases[J]? Diabetologia,1992,35:1181-1185.
  • 7[5]HOLE U,HARDING A E,MORGAN J A.Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies[J].Meurology,1988,331:717-719.
  • 8[6]WALACE D C,SINGH G,LOTT M T,et al.Mitochondrial DNA mutation assicited with Leber,s hereditary opticneuropathy[J].Science,1998,242:1427-1431.
  • 9[7]GOTO Y,NONAKA I,HORAI S.A mutation in the tRNAleu(uuR) gene associated with MELAS subgroup of mitochondrial encephalomyopathies[J].Nature,1990,348:651-655.
  • 10[8]SHOFFNER J M,LOTT M T,LEZZA A M S,et al.Myocloric epilepsy and ragged-redifiber disease (MERRF) is associated with a mitochondrial DNA tRNA lys mutation[J].Cell,1990,61:93-96.

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