טוען...
Living Donor Liver Transplantation in a Paediatric Patient With Citrullinaemia Type 2
Citrullinaemia is a urea cycle defect that results from a deficiency of the enzyme arginosuccinate synthetase. Type 1 disease is diagnosed in childhood, whereas type 2 disease is adult onset. But, we report the outcome in a boy (13 years) with citrullinaemia type 2 who received a live donor liver tr...
שמור ב:
| הוצא לאור ב: | J Clin Exp Hepatol |
|---|---|
| Main Authors: | , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Elsevier
2020
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7527851/ https://ncbi.nlm.nih.gov/pubmed/33029059 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jceh.2019.12.006 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|