期刊文献+

新疆地区苯丙酮尿症PAH基因新突变鉴定 被引量:4

下载PDF
导出
摘要 苯丙酮尿症(PKU)是一种常见的可以造成儿童不同程度智力损害的先天代谢性疾病,属于常染色体隐性遗传,其主要致病因素是苯丙氨酸羟化酶(PAH)基因的异常突变。这类突变包括所有外显子以及内含子、5'-UTR和3'-UTR区域等,突变的形式也多种多样,包括错义突变、小缺失、剪接位点突变、沉默突变、无义突变、小插入及大片段插入。
出处 《解放军医学杂志》 CAS CSCD 北大核心 2010年第12期1506-1507,共2页 Medical Journal of Chinese People's Liberation Army
  • 相关文献

参考文献7

  • 1Guldberg P, Romano V, Ceratto N, et al. Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in Southern Europe[J]. Hum Mol Genet,1993, 2(10): 1703- 1707.
  • 2Anderson OA, Flatmark T, Hough E. High resolution crystal structures of the catalytic domain of human phenylalanine hydroxylase in the catalytically active Fe (II) form and binary complex with tetra hydrohiopterin[J].J Mol Biol, 2001, 314(2):279-291.
  • 3Anderson OA, Flatmark T, Hough E. Crystal structure of the ternary complex of the catalytic domain of human phenylalanine hydroxylase with tetrahydrobiopterin and 3-(2-thienyl)-L-alanine, and its im plications for the mechanisms of catalysis and substrate activation[J]. J Mol Biol, 2002, 320(5): 1095-1108.
  • 4Pey AL, Desviat LR, Gdmez A, et al. Phenylketonuria: genotypephenotype correlations based on expression analysis of structural and functional mutations in PAH[J].Hum Mutat, 2003, 21 (4): 370- 378.
  • 5Guldberg P, Rey F, Zsehocke J, et al. A European multbcenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system forgenotype-based prediction of meta bolic phenotwe[J]. Am J Hum Genet, 1998. 63(1):71-79.
  • 6Zschocke J. Phenylketonuria mutations in Europe[J].Hum Mutat, 2003, 21(4) : 345-356.
  • 7Dobrowolski SF, Pey AL, Koch R, et al. Biochemical characterization of mutant phenylalanine hydroxylase enzymes and correlation with clinical presentation in hyperphenylalaninaemic patients[J]. J Inherit Metab Dis, 2009, 32(1):10-21.

同被引文献18

引证文献4

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部