Kidney Transplant in Fabry Disease: A Revision of the Literature
Fabry disease is classified as a rare X-linked disease caused by a complete or partial defect of enzyme alpha-galactosidase, due to <i>GLA</i> gene mutations. This disorder leads to intracellular globotriaosylceramide (Gb3) deposition associated with increased Gb3 plasma levels. Most of the symptoms...
保存先:
| 主要な著者: | , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI AG
2020-06-01
|
| シリーズ: | Medicina |
| 主題: | |
| オンライン･アクセス: | https://www.mdpi.com/1648-9144/56/6/284 |
| タグ: |
タグなし, このレコードへの初めてのタグを付けませんか!
|