Publikationsserver
Characterization of single point mutation in the gamma-carboxyglutamic acid domain of recombinant clotting Factor IX and its therapeutic potential
Hemophilia B (HB) is an inherited bleeding disorder caused by deficiency of FIX. The severity is classified based on the FIX activity level in the plasma. The trough levels of FIX activity in the circulation above 5% is considered the relevant parameter to maintain hemostasis. Even though rFIX produ...
Guardado en:
| Autor principal: | |
|---|---|
| Otros Autores: | |
| Formato: | Dissertation |
| Lenguaje: | inglés |
| Publicado: |
Philipps-Universität Marburg
2023
|
| Materias: | |
| Acceso en línea: | Texto Completo PDF |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Internet
Texto Completo PDF| Número de Clasificación: |
urn:nbn:de:hebis:04-z2023-03593 |
|---|---|
| Fecha de Publicación: |
2023-12-21 |
| Datum der Annahme: |
2023-04-27 |
| Downloads: |
50 (2024), 1 (2023) |
| Lizenz: |
https://rightsstatements.org/vocab/InC-NC/1.0/ |
| URL de Acceso: |
https://archiv.ub.uni-marburg.de/diss/z2023/0359 https://doi.org/10.17192/z2023.0359 |