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Amelioration of clinical disease following bone marrow transplantation in fucosidase-deficient dogs

✍ Scribed by Taylor, Rosanne M. ;Farrow, Brian R. H. ;Stewart, Graeme J.


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
613 KB
Volume
42
Category
Article
ISSN
0148-7299

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## Abstract ## Background Fabry disease (FD) is a lysosomal storage disorders characterized by a deficiency of the lysosomal enzyme, α‐galactosidase A. This results in the accumulation of glycolipids, mainly globotriaosylceramide (GL‐3), in the lysosomes of various organs. Although bone marrow tra