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.

Dades bibliogràfiques
Autor principal:	Eshaque, Tamannyat Binte
Altres autors:	Naser, Iftekhar Bin
Format:	Thesis
Idioma:	English
Publicat:	Brac University 2024
Matèries:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Accés en línia:	http://hdl.handle.net/10361/23983

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