Fabry disease: A single-center experience
Fabry disease (FD) is an inborn X-linked lysosomal storage disorder resulting from α–galactosidase A (α-Gal) activity deficiency in lysosomes. This results in the accumulation of particularly globotriaosylceramide (Gb3) within lysosomes in a wide variety of cells. This study aimed to analyze the cl...
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
National Kidney Foundation of Ukraine
2021-06-01
|
| Series: | Український Журнал Нефрології та Діалізу |
| Subjects: | |
| Online Access: | https://ukrjnd.com.ua/index.php/journal/article/view/492 |