Cargando…
P104: BASE EDITING REPAIRS THE HBE MUTATION RESTORING THE PRODUCTION OF NORMAL GLOBIN CHAINS IN SEVERE HBE/β-THALASSEMIA PATIENT HEMATOPOIETIC STEM AND ERYTHROID CELLS
Autores principales: | Badat, M, Hua, P, Mettananda, S, Fisher, C, Roy, N, Rice, S, Roy, A, Higgs, D, Davies, J |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811873/ http://dx.doi.org/10.1097/01.HS9.0000821508.47147.52 |
Ejemplares similares
-
Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia
por: Mettananda, Sachith, et al.
Publicado: (2017) -
Impaired Terminal Erythroid Maturation in β(0)-Thalassemia/HbE Patients with Different Clinical Severity
por: Suriyun, Thunwarat, et al.
Publicado: (2022) -
Moyamoya syndrome in a child with HbEβ‐thalassemia
por: Zahra, Akmal, et al.
Publicado: (2022) -
Predictive SNPs for β(0)-thalassemia/HbE disease severity
por: Munkongdee, Thongperm, et al.
Publicado: (2021) -
Abstract 40: Adrenal insufficiency in patients with HbE/Beta thalassemia
por: Singh, Arijit, et al.
Publicado: (2022)