Trial Interviews to Explore Glycogen Storage Disease Type Ia Patient Experiences Following Gene Therapy
# Background Glycogen storage disease type Ia (GSDIa) is a rare, inherited, autosomal recessive deficiency of glucose-6-phosphatase (G6Pase), an enzyme necessary in glycogenolysis and gluconeogenesis. To maintain normal blood glucose levels and ensure survival, individuals living with GSDIa must fre...
Tallennettuna:
| Päätekijät: | , , , , , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Columbia Data Analytics, LLC
2026-02-01
|
| Sarja: | Journal of Health Economics and Outcomes Research |
| Linkit: | https://doi.org/10.36469/001c.155666 |
| Tagit: |
Ei tageja, Lisää ensimmäinen tagi!
|