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.

Dettagli Bibliografici
Autore principale:	Eshaque, Tamannyat Binte
Altri autori:	Naser, Iftekhar Bin
Natura:	Tesi
Lingua:	English
Pubblicazione:	Brac University 2024
Soggetti:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Accesso online:	http://hdl.handle.net/10361/23983

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