Advances and challenges in phenylketonuria

被引：10

作者：

Harding, Cary O. ^{[1
,2
]}

Blau, Nenad ^{[3
,4
]}

机构：

[1] Oregon Hlth & Sci Univ, Dept Mol & Med Genet, Portland, OR 97201 USA

[2] Oregon Hlth & Sci Univ, Dept Pediat, Portland, OR 97201 USA

[3] Univ Childrens Hosp, Div Clin Chem & Biochem, Zurich, Switzerland

[4] Zurich Ctr Integrat Human Physiol ZIHP, Zurich, Switzerland

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 2010年 / 33卷 / 06期

关键词：

PHENYLALANINE-HYDROXYLASE DEFICIENCY; MURINE PHENYLKETONURIA; MOUSE MODEL; AMMONIA-LYASE; GENE-TRANSFER; TETRAHYDROBIOPTERIN; MUTATIONS; THERAPY; HYPERPHENYLALANINEMIA; RESPONSIVENESS;

D O I：

10.1007/s10545-010-9247-7

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：645 / 648

页数：4

共 29 条

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