Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency (vol 29, pg 167, 2008)

被引：0
|
作者：
Zurflueh, Marcel R. [1 ]
Zschocke, Johannes [2 ]
Lindner, Martin [3 ]
Feillet, Francois [4 ]
Chery, Celine [4 ]
Burlina, Alberto [5 ]
Stevens, Raymond C. [6 ]
Thoeny, Beat [1 ]
Blau, Nenad
机构：
[1] Univ Childrens Hosp, Div Clin Chem & Biochem, CH-8032 Zurich, Switzerland
[2] Univ Heidelberg, Inst Human Genet, Heidelberg, Germany
[3] Univ Heidelberg, Dept Pediat, Div Metab Disorders, Heidelberg, Germany
[4] Hop Enfants, Ctr Reference Malad Hereditaires Metab, Vandoeuvre Les Nancy, France
[5] Univ Hosp, Dept Pediat, Div Metab Disorders, Padua, Italy
[6] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
来源：
HUMAN MUTATION | 2008年 / 29卷 / 08期
关键词：
D O I：
10.1002/humu.20821
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
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页码：1079 / 1079
页数：1
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