Fabry Disease
Fabry disease is an X-linked inborn error of metabolism wherein deficiency of a lysosomal enzyme results in systemic deposition of glycosphingolipids. Storage deposition, and hence pathological disease, occurs preferentially in renal glomerular and tubular epithelial cells, myocardial cells, heart v...
| Corporate Author: | SpringerLink (Online service) |
|---|---|
| Other Authors: | Elstein, Deborah (Editor), Altarescu, Gheona (Editor), Beck, Michael (Editor) |
| Format: | Electronic eBook |
| Language: | English |
| Published: |
Dordrecht :
Springer Netherlands : Imprint: Springer,
2010.
|
| Subjects: | |
| Online Access: | Full Text via HEAL-Link |
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