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

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