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四氢生物蝶呤反应性的苯丙酮尿症研究进展 被引量:3

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摘要 本文综述对四氢生物蝶呤(BH4)反应性的苯丙氨酸羟化酶(PAH)基因缺陷的苯丙酮尿症(PKU)的研究进展。分析BH4反应性的PAH基因突变,探讨这一现象潜在的发生机制,介绍一种新的临床分类法,并对PKU的BH4替代治疗前景进行展望。
作者 瞿宇晋 宋昉
出处 《国外医学(遗传学分册)》 2005年第4期253-256,F0003,共5页 Foreign Medical Sciences(Section of Genetics )
基金 国家重点基础性研究973项目(No.2001CB510306)
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参考文献21

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同被引文献25

  • 1殷惠芳,杨宏莉.保定地区19例苯丙酮尿症患者调查结果分析[J].中国优生与遗传杂志,2008,16(10). 被引量:5
  • 2侯岚,高媛,宋利.苯丙酮尿症的研究进展[J].中国实用医药,2007,2(24):116-118. 被引量:9
  • 3Hvas AM,Nexo E,Nielsen JB.Vitamin B2and vitamin B6sup-plementation is needed among adults with phenylketonuria(PKU)[J].Journalof Inherited Metabolic Disease,2006,29(1):47-53. 被引量:1
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  • 7卫生部办公厅.卫妇社发[2010]96号.新生儿疾病筛查技术规范[S]. 2010-11-10. 被引量:1
  • 8广东省卫生厅.粤卫[2008]228号.广东省新生儿疾病筛査管理办法[S]. 2008-01-16. 被引量:1
  • 9van Spronsen FJ. Mild hyperphenylalaninemia : to treat ornot to treat [J]. J Inherit Metab Dis,2011,34 (3) : 651-656. 被引量:1
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