Two ''new'' treatable inherited biosynthetic disorders

被引:2
作者
Walter, JH
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D O I
10.1016/S0140-6736(05)64790-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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页码:558 / 559
页数:2
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共 4 条
[1]   Cloning and sequence analysis of human guanidinoacetate N-methyltransferase cDNA [J].
Isbrandt, D ;
vonFigura, K .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1995, 1264 (03) :265-267
[2]   3-phosphoglycerate dehydrogenase deficiency: An inborn error of serine biosynthesis [J].
Jaeken, J ;
Detheux, M ;
VanMaldergem, L ;
Foulon, M ;
Carchon, H ;
VanSchaftingen, E .
ARCHIVES OF DISEASE IN CHILDHOOD, 1996, 74 (06) :542-545
[3]  
STOCKLER S, 1994, PEDIATR RES, V36, P409
[4]  
STOCKLER S, 1996, AM J HUM GENET, V59, P914