Human glycosylation disorders and sugar supplement therapy

被引：20

作者：

Freeze, HH ^{[1
]}

机构：

[1] Burnham Inst, La Jolla, CA 92037 USA

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1999年 / 255卷 / 02期

关键词：

D O I：

10.1006/bbrc.1998.9945

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Some genetic defects in protein glycosylation can be treated effectively with dietary supplements of monosaccharides. An easy screening test and non-toxic therapy for potentially lethal disorders should encourage physicians to search for more patients with glycosylation disorders. It should also stimulate research on the occurrence and availability of monosaccharides used for glycoconjugate synthesis and for vertebrate models to Study their utilization. (C) 1999 Academic Press.

引用

页码：189 / 193

页数：5

共 69 条

[61] CARBOHYDRATE-DEFICIENT SERUM TRANSFERRIN IN A NEW SYSTEMIC HEREDITARY SYNDROME [J].