A case of benign pyruvate carboxylase deficiency with normal development

被引：20

作者：

Hamilton, J ^{[1
]}

Rae, MD ^{[1
]}

Logan, RW ^{[1
]}

Robinson, PH ^{[1
]}

机构：

[1] ROYAL HOSP SICK CHILDREN,YORKHILL NHS TRUST,DEPT CHILD HLTH,GLASGOW G3 8SJ,LANARK,SCOTLAND

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1997年 / 20卷 / 03期

关键词：

D O I：

10.1023/A:1005350600278

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

收藏

页码：401 / 403

页数：3

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[J]. PEDIATRIC RESEARCH, 1979, 13 (01) : 38 - 43
[2] PYRUVATE-CARBOXYLASE DEFICIENCIES - COMPLEMENTATION STUDIES BETWEEN FRENCH AND AMERICAN PHENOTYPES IN CULTURED FIBROBLASTS
AUGEREAU, C
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MARSAC, C
SAUDUBRAY, JM
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[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1985, 8 (02) : 59 - 62
[3] Sly W. S., 1995, METABOLIC MOL BASES, P1479
[4] VANCOSTER RN, 1991, PEDIATR RES, V30, P1