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.

Détails bibliographiques
Auteur principal:	Eshaque, Tamannyat Binte
Autres auteurs:	Naser, Iftekhar Bin
Format:	Thèse
Langue:	English
Publié:	Brac University 2024
Sujets:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Accès en ligne:	http://hdl.handle.net/10361/23983

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