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.

Bibliografiset tiedot
Päätekijä: Ullah, Mohammad
Muut tekijät: Islam, Farzana
Aineistotyyppi: Opinnäyte
Kieli:English
Julkaistu: Brac University 2023
Aiheet:
SCD
CRISPR/Cas9
Hematopoietic stem/progenitor cells
Fetal hemoglobin
Gene editing tools
Genetic engineering > Research
Gene therapy > Research
Biotechnology
Linkit:http://hdl.handle.net/10361/19355

Internet

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

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