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.

Библиографические подробности
Главный автор:	Eshaque, Tamannyat Binte
Другие авторы:	Naser, Iftekhar Bin
Формат:	Диссертация
Язык:	English
Опубликовано:	Brac University 2024
Предметы:	Duchenne muscular dystrophy Multiplex PCR Exon X-linked recessive disorder Duchenne muscular dystrophy. Genetic disorder.
Online-ссылка:	http://hdl.handle.net/10361/23983

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