𝔖 Bobbio Scriptorium
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Investigation of the α-Galactosidase Deficiency in Fabry's Disease Using Antibodies against the Purified Enzyme

✍ Scribed by Peter J. G. M. RIETRA; Joseph M. TAGER; Piet BORST; Jacques L. MOLENAAR; Michiel N. HAMERS

Book ID
115114227
Publisher
John Wiley and Sons
Year
1974
Tongue
English
Weight
995 KB
Volume
46
Category
Article
ISSN
1432-1327

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Partial correction of the α-galactosidase A deficiency and reduction of glycolipid storage in Fabry mice using synthetic vectors
✍ Malgorzata Przybylska; I-Huan Wu; Hongmei Zhao; Robin J. Ziegler; Jennifer D. To 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 163 KB

## Abstract ## Background Fabry disease is a recessive, X‐linked disorder caused by a deficiency of the lysosomal enzyme α‐galactosidase A, leading to an accumulation of the glycosphingolipid globotriaosylceramide (GL‐3) in most tissues of the body. The goal of this study was to determine if syste