CRISPR/Cas9 genome editing to treat sickle cell disease

CRISPR/Cas9 genome editing to treat sickle cell disease

This thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2022.

Bibliografski detalji
Glavni autor: Ullah, Mohammad
Daljnji autori: Islam, Farzana
Format: Disertacija
Jezik:English
Izdano: Brac University 2023
Teme:
SCD
CRISPR/Cas9
Hematopoietic stem/progenitor cells
Fetal hemoglobin
Gene editing tools
Genetic engineering > Research
Gene therapy > Research
Biotechnology
Online pristup:http://hdl.handle.net/10361/19355

Internet

http://hdl.handle.net/10361/19355

Similar Items