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.

Bibliografske podrobnosti
Glavni avtor:	Eshaque, Tamannyat Binte
Drugi avtorji:	Naser, Iftekhar Bin
Format:	Thesis
Jezik:	English
Izdano:	Brac University 2024
Teme:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Online dostop:	http://hdl.handle.net/10361/23983

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