EXCRETION OF MANNOSE-RICH COMPLEX CARBOHYDRATES BY A PATIENT WITH ALPHA-MANNOSIDASE DEFICIENCY (MANNOSIDOSIS)

被引：37

作者：

TSAY, GC

DAWSON, G

MATALON, R

机构：

[1] UNIV CHICAGO, JOSEPH P KENNEDY JR MENTAL RETARDATION RES CTR, DEPT BIOCHEM, CHICAGO, IL 60637 USA

[2] UNIV CHICAGO, JOSEPH P KENNEDY JR MENTAL RETARDATION RES CTR, DEPT PEDIAT, 950 E59TH ST, CHICAGO, IL 60637 USA

来源：

JOURNAL OF PEDIATRICS | 1974年 / 84卷 / 06期

关键词：

D O I：

10.1016/S0022-3476(74)80768-7

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：865 / 868

页数：4

共 11 条

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[2] LACTOSYLCERAMIDOSIS - LACTOSYLCERAMIDE GALACTOSYL HYDROLASE DEFICIENCY AND ACCUMULATION OF LACTOSYLCERAMIDE IN CULTURED SKIN FIBROBLASTS [J].

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STEIN, AO .

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[3] DEFICIENCY OF ALPHA-MANNOSIDASE IN ANGUS CATTLE - INHERITED LYSOSOMAL STORAGE-DISEASE [J].

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MATALON R, TO BE PUBLISHED

[5] URINARY MANNOSE IN MANNOSIDOSIS [J].

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OCKERMAN, PA ;

SZABO, L .

JOURNAL OF PEDIATRICS, 1973, 82 (04) :686-688

[6] MANNOSIDOSIS IN ANGUS CATTLE - PARTIAL CHARACTERIZATION OF 2 MANNOSE CONTAINING OLIGOSACCHARIDES [J].

NORDEN, NE ;

LUNDBLAD, A ;

OCKERMAN, PA ;

JOLLY, RD .

FEBS LETTERS, 1973, 35 (02) :209-212

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NORDEN NE, 1973, J BIOL CHEM, V248, P6210

[8]

OBRIEN JS, 1972, METABOLIC BASIS INHE

[9]

OCKERMAN PA, 1967, LANCET, V2, P239

[10]

OCKERMAN PA, 1973, LYSOSOMES STORAGE DI, pCH11

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