CDG nomenclature: Time for a change!

被引：117

作者：

Jaeken, Jaak ^{[1
]}

Hennet, Thierry ^{[2
]}

Matthijs, Gert ^{[3
]}

Freeze, Hudson H. ^{[4
]}

机构：

[1] Katholieke Univ Leuven, Ctr Metab Dis, BE-3000 Louvain, Belgium

[2] Univ Zurich, Inst Physiol, CH-8057 Zurich, Switzerland

[3] Katholieke Univ Leuven, Ctr Human Genet, BE-3000 Louvain, Belgium

[4] Burnham Inst Med Res, La Jolla, CA 92037 USA

来源：

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2009年 / 1792卷 / 09期

关键词：

CONGENITAL DISORDERS; GLYCOSYLATION; DEFICIENCY; SERUM;

D O I：

10.1016/j.bbadis.2009.08.005

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

070307 [化学生物学]; 071010 [生物化学与分子生物学];

摘要：

[No abstract available]

引用

页码：825 / 826

页数：2

共 12 条

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[8]

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