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.

Bibliografiska uppgifter
Huvudupphovsman:	Eshaque, Tamannyat Binte
Övriga upphovsmän:	Naser, Iftekhar Bin
Materialtyp:	Lärdomsprov
Språk:	English
Publicerad:	Brac University 2024
Ämnen:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Länkar:	http://hdl.handle.net/10361/23983

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