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...
| Συγγραφή απο Οργανισμό/Αρχή: | SpringerLink (Online service) |
|---|---|
| Άλλοι συγγραφείς: | Elstein, Deborah (Επιμελητής έκδοσης), Altarescu, Gheona (Επιμελητής έκδοσης), Beck, Michael (Επιμελητής έκδοσης) |
| Μορφή: | Ηλεκτρονική πηγή Ηλ. βιβλίο |
| Γλώσσα: | English |
| Έκδοση: |
Dordrecht :
Springer Netherlands : Imprint: Springer,
2010.
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| Θέματα: | |
| Διαθέσιμο Online: | Full Text via HEAL-Link |
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Laboratory Guide to the Methods in Biochemical Genetics
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Physician’s Guide to the Treatment and Follow-Up of Metabolic Diseases
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Oxidative Phosphorylation in Health and Disease
ανά: Smeitink, Jan A. M., κ.ά.
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Nutrition Management of Inherited Metabolic Diseases Lessons from Metabolic University /
Έκδοση: (2015)