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.

Bibliografiske detaljer
Hovedforfatter:	Eshaque, Tamannyat Binte
Andre forfattere:	Naser, Iftekhar Bin
Format:	Thesis
Sprog:	English
Udgivet:	Brac University 2024
Fag:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Online adgang:	http://hdl.handle.net/10361/23983

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