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.

Opis bibliograficzny
1. autor:	Eshaque, Tamannyat Binte
Kolejni autorzy:	Naser, Iftekhar Bin
Format:	Praca dyplomowa
Język:	English
Wydane:	Brac University 2024
Hasła przedmiotowe:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Dostęp online:	http://hdl.handle.net/10361/23983

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