THE MUTATION SPECTRUM OF PHENYLALANINE HYDROXYLASE DEFICIENCY IN CYPRUS

被引：0
|
作者：
Georgiou, Th [1 ]
Ho, G. [2 ,3 ]
Dionysiou, M. [1 ]
Nicolaou, A. [4 ]
Vogazianos, M. [4 ]
Chappa, G. [5 ]
Stylianidou, G. [5 ]
Christodoulou, J. [2 ,3 ]
Drousiotou, A. [1 ]
机构：
[1] Cyprus Inst Neurol & Genet, Dept Biochem Genet, Nicosia, Cyprus
[2] Childrens Hosp, Genet Metab Dis Res Unit, Westmead, NSW, Australia
[3] Univ Sydney, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia
[4] Ctr Prevent Paediat, Limassol, Cyprus
[5] Archbishop Makarios III Hosp, Dept Paediat Neurol, Nicosia, Cyprus
来源：
MOLECULAR GENETICS AND METABOLISM | 2009年 / 98卷 / 1-2期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
188
引用
收藏
页码：24 / 24
页数：1
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