A novel sequence of the PHKG2 mutation associated with the first case of glycogen storage diseases type IXc in Syria: a case report and review of literature
المصدر: Journal of Medical Case Reports
| المجلد | 19 |
|---|---|
| العدد | 1 |
| DOI | 10.1186/s13256-025-05383-z |
| نوع المنشور | مقالة دورية |
| الفهرسة | Scopus |