Minimum requirement of donor cells to re
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Takayuki Yokoi; Hiroshi Kobayashi; Yohta Shimada; Yoshikatsu Eto; Nobuyuki Ishig
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Article
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2011
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John Wiley and Sons
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English
⚖ 229 KB
## 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