Exploring of deletion mutation causative for Duchenne Muscular Dystrophy (DMD) in Bangladesh cohort
This thesis is submitted in partial fulfillment of the requirement for the degree of Master of Science in Biotechnology, 2022.
Autor Principal: | Eshaque, Tamannyat Binte |
---|---|
Outros autores: | Naser, Iftekhar Bin |
Formato: | Thesis |
Idioma: | English |
Publicado: |
Brac University
2024
|
Subjects: | |
Acceso en liña: | http://hdl.handle.net/10361/23983 |
Títulos similares
-
A review on the rare diseases and subsequent orphan drugs
por: Oishi, Nuzhat Anjum
Publicado: (2024) -
Review on gene replacement therapy for spinal muscular atrophy
por: Jannat, Nurani
Publicado: (2023) -
A review on spinal muscular atrophy - a fetal autosomal neurotransmitter recessive disorder
por: Tabassum, Nafiza
Publicado: (2024) -
Restless Legs Syndrome: a review from causation to cure
por: Rahman, Mustafizur
Publicado: (2024) -
CRISPR: a revolutionary tool for modeling and treating cancer and Duchenne muscular dystrophy
por: Eva, Israt Ara Jannat
Publicado: (2023)