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
| Title: | 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 |
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| Authors: | Harh, SebaAff1, IDs1325602505383z_cor1; Shahoud, ShazaAff1; Daher, ShadyAff1; Alasmar, DianaAff2 |
| Source: | Journal of Medical Case Reports. 19(1) |
| Database: | Springer Nature Journals |