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...

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Bibliographic Details
Other Involved Persons: Elstein, Deborah (Other) ; Altarescu, Gheona (Other) ; Beck, Michael (Other)
Format: eBook
Language:English
Published: Dordrecht : Springer Science+Business Media B.V 2010
ISBN:9789048190331
9048190339
9789048190324
9048190320
Item Description:Includes bibliographical references and index
Physical Description:Online-Ressource v.: digital
DOI:10.1007/978-90-481-9033-1
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Other Editions:Show all 2 Editions
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