Proteomics of specific treatment-related alterations in Fabry disease: A strategy to identify biological abnormalities

Fabry disease is inherited as an X-linked disorder secondary to deficiency of α-galactosidase A, resulting in abnormal metabolism of substances containing α-d-galactosyl moieties. As a consequence, a multisystem disorder develops, culminating in strokes, progressive renal, and cardiac dysfunction. S...

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Detaylı Bibliyografya
Asıl Yazarlar: Moore, David F., Krokhin, Oleg V., Beavis, Ronald C., Ries, Markus, Robinson, Chevalia, Goldin, Ehud, Brady, Roscoe O., Wilkins, John A., Schiffmann, Raphael
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2007
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1797627/
https://ncbi.nlm.nih.gov/pubmed/17301227
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0611315104
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