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.

Dades bibliogràfiques
Autor principal:	Ullah, Mohammad
Altres autors:	Islam, Farzana
Format:	Thesis
Idioma:	English
Publicat:	Brac University 2023
Matèries:	SCD CRISPR/Cas9 Hematopoietic stem/progenitor cells Fetal hemoglobin Gene editing tools Genetic engineering > Research Gene therapy > Research Biotechnology
Accés en línia:	http://hdl.handle.net/10361/19355

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