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.

Bibliografski detalji
Glavni autor:	Eshaque, Tamannyat Binte
Daljnji autori:	Naser, Iftekhar Bin
Format:	Disertacija
Jezik:	English
Izdano:	Brac University 2024
Teme:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Online pristup:	http://hdl.handle.net/10361/23983

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