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.

Podrobná bibliografie
Hlavní autor:	Eshaque, Tamannyat Binte
Další autoři:	Naser, Iftekhar Bin
Médium:	Diplomová práce
Jazyk:	English
Vydáno:	Brac University 2024
Témata:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
On-line přístup:	http://hdl.handle.net/10361/23983

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