Exploring of deletion mutation causative for Duchenne Muscular Dystrophy (DMD) in Bangladesh cohort

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.

Manylion Llyfryddiaeth
Prif Awdur:	Eshaque, Tamannyat Binte
Awduron Eraill:	Naser, Iftekhar Bin
Fformat:	Traethawd Ymchwil
Iaith:	English
Cyhoeddwyd:	Brac University 2024
Pynciau:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Mynediad Ar-lein:	http://hdl.handle.net/10361/23983

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